Recalls: Other Drugs or Medications

This recall involves the ALOCANE® Emergency Burn Pads (10 count and 15 count) which come in a white and red box with "MAXIMUM STRENGTH ALOCANE® Emergency Burn Pads" printed on the front. The product is an over the counter Gel Infused Pad with lidocaine (4%) as the active ingredient. The pads are sold in a 10 count box and 15 count box with the lot numbers 4179, 4180, 4235, 4645, 4646 or 4698 printed next to the barcode on the box. The UPC number for the affected product is 8-46241-02448-7 and can be found on the bottom of the box. Read more.

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 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 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 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.

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.

The recalled Synodrin Lidocaine Maximum Strength Pain Relieving Cream is in a white jar with a blue label with "Synodrin Lidocaine Maximum Strength 4% Pain Relieving Cream" printed on the front. The jars measure about three inches in diameter, are three inches tall and weigh about 4 ounces. They were sold in a blue box with yellow letters "Lidocaine" and white letters "Maximum Strength 4% Pain Relieving Cream." The brand name Synodrin is printed on the jar and the box. The box and jar have UPC code 8 64751 00032 6 printed on the right side. Read more.