Label: ANTIBIOTIC AND PAIN RELIEF- bacitracin, neomycin, polymyxin b, pramoxine hcl ointment
- NDC Code(s): 11822-0444-1, 11822-0444-2, 11822-0444-3
- Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated June 8, 2017
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients (in each gram)
- Purpose
- Uses
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Warnings
For external use only.
Do not use
- •
- if you are allergic to any of the ingredients
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- in the eyes
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- over large areas of the body
- Directions
- Other information
- Inactive ingredient
- Questions or comments?
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Principal Display Panel
Compare to the active ingredients of Neosporin® + Pain Relief
MAXIMUM STRENGTH
first aid antibiotic + pain relief ointment
bacitracin zinc – neomycin sulfate – polymyxin B sulfate – pramoxine HCl
first aid antibiotic/pain relieving ointment
helps prevent infection and for temporary relief of pain due to minor cuts, scrapes and burns
NET WT 1 OZ (28 g)
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INGREDIENTS AND APPEARANCE
ANTIBIOTIC AND PAIN RELIEF
bacitracin, neomycin, polymyxin b, pramoxine hcl ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-0444 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 500 [USP'U] in 1 g NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN 3.5 mg in 1 g POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B 10000 [USP'U] in 1 g PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE 10 mg in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) Product Characteristics Color YELLOW (Translucent) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-0444-1 1 in 1 CARTON 02/18/2009 1 14 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:11822-0444-2 1 in 1 CARTON 08/17/2005 2 28 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:11822-0444-3 2 in 1 CARTON 06/08/2017 3 28 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333B 08/17/2005 Labeler - Rite Aid Corporation (014578892)