Recalls: Drugs and Cosmetics

The recalled PipingRock wintergreen 100% pure essential oil is in a 1/2 fl. oz. (15 ml) glass amber dropper bottle. It has a black cap and a yellow, red and green label with PipingRock Wintergreen Oil Gaultheria procumbens 100% Pure Essential Oil printed on the front. Product number NT6446, UPC code 610256764467 and lot number 1905, 4000, 5980, 7420, 9344, 11202, 27180, 31397, 37913, 43369, 45843 or 56439 are printed on the back of the product. Read more.

This recall involves EZY Gel Topical Anesthetic Gel. The recalled product was sold in 1 fluid ounce white bottles. Biotouch Topical Anesthetic Gel EZY Gel is printed on a purple label located on the front panel. Lot numbers and expiration dates are located on the bottom of the bottle. Read more.

This recall involves Numb 100 Topical Anesthetic Cream. The recalled cream is in a 1.35 fluid ounce white jar with a rounded cap. Numb 100 Topical Anesthetic Cream and a blue cross are printed on the jar's front panel. Read more.

This recall involves Women's Iron Complete Dietary Supplement 60-count caplets. The recalled dietary supplement is in a white box with "Women's Iron Complete" printed on the front in gray and red font. The box contains blister packets with a total of sixty caplets. Read more.

This recall involves all Pain Relief Naturally lidocaine-containing products including Numbify, Extra Strength Numbify, Pre-TAT Tattoo, Superior Pain & Itch Relief, and Soothing Sore Relief creams, sprays, gels and liquid gels. The recalled products were sold in 1, 2 and 4 ounce size containers. The products have black packaging with the name of the product in gold, red, or green lettering. Numbify Cream, Spray, Gel & Liquid Gel Black tubs and bottles with gold lettering Extra Strength Numbify Cream, Spray, Gel & Liquid Gel Black tubs and bottles with gold lettering Pre-TAT Tattoo Cream, Spray, Gel & Liquid Gel Black tubs and bottles with red lettering Superior Pain & Itch Relief Cream, Spray, Gel & Liquid Gel Black tubs and bottles with green lettering Soothing Sore Relief Cream, Spray, Gel & Liquid Gel Black tubs and bottles with green lettering Read more.

This recall involves UberScientific Uber Numb Topical Anesthetic Cream and Uber Numb Spray. The recalled cream is in a white jar with a smooth, rounded cap and a green label with "Uber Numb Topical Anesthetic Cream" printed on the front. The cream was sold in one, two and four ounce sizes with the lot numbers printed on the bottom of the jar and the UPC number printed on the label to the left of the product name. The brand name UberScientific is printed on the label below the net weight. The recalled spray is in a green bottle with a white cap and has a white label with "Uber Numb Spray" printed on the front. The spray was sold in four ounce size with the lot numbers printed on the bottom of the bottle and the UPC number printed on the label to the right of the product name. The brand name UberScientific is printed on the label to the left of the product name. Product Size UPC Lot Numbers UberScientific Uber Numb Topical Anesthetic Cream 1 oz. 00863255000306 A23Z3 and F12Z5 2 oz. 00863255000344 L06Z2A, L06Z2B, and B01N2A 4 oz. 0083255000313 E10Z4, L06Z2, and B01N2 Uber Numb Spray 4 oz. 00850777008002 K30Z6 and B09N2 Read more.

The recalled Desert Harvest Reléveum Skin Repair Cream is in a transparent green bottle with a white pump dispenser cap and a tan/white gradient label with "Desert Harvest Reléveum" printed on the front. The product is an over the counter skin cream with lidocaine (4%) as the active ingredient. The cream is sold in a 4 ounce or an 8 ounce bottle with the date code "D02N5" printed above the barcode on the bottle. Read more.

This recall involves blister packages of prescription drugs from Novartis and Sandoz. The drugs are packaged with 3 to 10 tablets per blister card. The recalled Novartis prescription blister packages have "Novartis," the name of the drug, dosage, NDC, lot number and expiration date printed on the cartons and the blister cards. The recall includes the following: Recalled Novartis Prescription Drugs NDC Numbers Tablet Strength Carton Configuration Lot Numbers Expiration Date Zofran ODT® 0078-0679-61 0078-0679-19 4 mg 30 count: 3 cards with 10 tablets each 1657088 Dec 2019 Zofran ODT® 0078-0680-61 0078-0680-19 8 mg 30 count: 3 cards with 10 tablets each 1641546 Oct 2019 Entresto® (sacubitril/valsartan) 0078-0659-61 0078-0659-35 24 mg/ 26 mg 100 count: 10 cards with 10 tablets each FX000005 FX000004 FX000003 F0010 F0009 F0007 Apr 2020 Apr 2020 Sep 2019 Nov 2018 Aug 2018 Jul 2018 Entresto® (sacubitril/valsartan) 0078-0777-61 0078-0777-35 49 mg/ 51 mg 100 count: 10 cards with 10 tablets each FX000001 F0006 F0005 F0004 Dec 2019 Oct 2019 Aug 2019 Oct 2018 Entresto® (sacubitril/valsartan) 0078-0696-61 0078-0696-35 97 mg/ 103 mg 100 count: 10 cards with 10 tablets each FX000002 F0007 F0006 F0005 F0004 Mar 2020 Feb 2020 Dec 2019 Dec 2018 Oct 2018 The recalled Sandoz prescription blister packages have "Sandoz," the name of the drug, dosage, NDC and lot number printed on the cartons and the blister cards. Lot numbers are listed at www.us.sandoz.com/patients-customers/product-safety-notices. The recall includes the following: Recalled Sandoz Prescription Drugs Tablet Strength NDC Numbers Carton Configuration Azithromycin Tablets 250 mg 0781-5776-06 0781-5776-69 50 count: 5 cards with 10 tablets each Donepezil ODT Tablets 5 mg 0781-5276-06 0781-5276-64 30 count: 3 cards with 10 tablets each Donepezil ODT Tablets 10 mg 0781-5277-06 0781-5277-64 30 count: 3 cards with 10 tablets each Haloperidol Tablets 0.5 mg 0781-1391-13 100 count: 10 cards with 10 tablets each Haloperidol Tablets 1 mg 0781-1392-13 100 count: 10 cards with 10 tablets each Haloperidol Tablets 2 mg 0781-1393-13 100 count: 10 cards with 10 tablets each Haloperidol Tablets 5 mg 0781-1396-13 100 count: 10 cards with 10 tablets each Haloperidol Tablets 10 mg 0781-1397-13 100 count: 10 cards with 10 tablets each Imipramine HCl Tablets 25 mg 0781-1764-13 100 count: 10 cards with 10 tablets each Imipramine HCl Tablets 50 mg 0781-1766-13 100 count: 10 cards with 10 tablets each Isosorbide Dinitrate (ISDN) Tablets 10 mg 0781-1556-13 100 count: 10 cards with 10 tablets each Isosorbide Dinitrate (ISDN) Tablets 20 mg 0781-1695-13 100 count: 10 cards with 10 tablets each Naratriptan Tablets 2.5 mg 0781-5527-06 0781-5527-37 9 count: 1 card with 9 tablets Ondansetron Tablets 8 mg 0781-1681-33 3 count: 1 card with 3 tablets Ondansetron ODT 4 mg 0781-5238-06 0781-5238-64 30 count: 3 cards with 10 tablets each Ondansetron ODT 8 mg 0781-5239-06 0781-5239-64 30 count: 3 cards with 10 tablets each Ondansetron ODT 8 mg 0781-5239-06 0781-5239-80 10 count: 1 card with 10 tablets Perphenazine Tablets 2 mg 0781-1046-13 100 count: 10 cards with 10 tablets each Perphenazine Tablets 4 mg 0781-1047-13 100 count: 10 cards with 10 tablets each Perphenazine Tablets 8 mg 0781-1048-13 100 count: 10 cards with 10 tablets each Risperidone ODT 0.5 mg 0781-5310-06 0781-5310-08 28 count: 7 cards with 4 tablets each Risperidone ODT 1 mg 0781-5311-06 0781-5311-08 28 count: 7 cards with 4 tablets each Risperidone ODT 2 mg 0781-5312-06 0781-5312-08 28 count: 7 cards with 4 tablets each Risperidone ODT 3 mg 0781-5313-06 0781-5313-08 28 count: 7 cards with 4 tablets each Risperidone ODT 4 mg 0781-5314-06 0781-5314-08 28 count: 7 cards with 4 tablets each Read more.

This recall involves Maximum Strength Bacitraycin Plus Ointment with Lidocaine. The recalled ointment is in a white, one ounce tube with "Bacitraycin Plus" printed on the front in green. Lidocaine is one of the two active ingredients listed on the back of the tube. The tube measures approximately 5 inches long by 1 inch wide. The lot number is printed on the end of the tube. The following lot numbers are included in the recall: Lot Numbers 16001 through 16002 404001 through 404002 405001 through 405003 406001 through 406004 407001 through 407002 415001 through 415010 416001 through 416003 417001 through 417004 Read more.

The recalled Well at Walgreens Pain and Itch Relief Cream tube and packaging are orange with a purple stripe with "Maximum Strength," "Pain and Itch Relief Cream 4% Lidocaine" and "NET WT 2 OZ (56.7 grams)" printed in white on the front. The Well at Walgreens logo is located on the front upper right corner. The packaging contains the UPC bar code 3 11917 18962 8 on the back. Read more.