Label: FIRST AID TRIPLE ANTIBIOTIC PAIN AND SCAR- bacitracin zinc, neomycin sulfate, polymyxin b, pramoxine hcl ointment
- NDC Code(s): 11822-0703-1, 11822-0703-2
- 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 January 16, 2018
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- Official Label (Printer Friendly)
- Active ingredients (in each gram)
- Purpose
- Uses
- Warnings
- Do not use
- Ask a doctor before use if you have
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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Package/Label Principal Display Panel
Compare to the active ingredients of Neosporin® + Pain Itch Scar
first aid
triple antibiotic pain + scar ointment
bacitracin zinc
neomycin sulfate
polymyxin B sulfate
pramoxine HCl
first aid antibiotic/pain relieving ointment
pain – itch – scar ointment – long lasting infection protection
minimizes the appearance of scars
NET WT 0.5 OZ (14 g)
first aid
triple antibiotic pain + scar ointment
bacitracin zinc
neomycin sulfate
polymyxin B sulfate
pramoxine HCl
first aid antibiotic/pain relieving ointment
powerful pain and itch relief for minor cuts, scrapes and burns
NET WT 0.5 OZ (14 g)
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INGREDIENTS AND APPEARANCE
FIRST AID TRIPLE ANTIBIOTIC PAIN AND SCAR
bacitracin zinc, neomycin sulfate, polymyxin b, pramoxine hcl ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-0703 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 COCOA BUTTER (UNII: 512OYT1CRR) OLIVE OIL (UNII: 6UYK2W1W1E) PETROLATUM (UNII: 4T6H12BN9U) SODIUM PYRUVATE (UNII: POD38AIF08) COTTONSEED OIL (UNII: H3E878020N) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Product Characteristics Color YELLOW (Pale) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-0703-1 1 in 1 CARTON 03/09/2017 1 14 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:11822-0703-2 1 in 1 CARTON 01/16/2018 2 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 03/09/2017 Labeler - Rite Aid Corporation (014578892)