Label: ANTIBIOTIC PLUS PAIN RELIEF MAXIMUM STRENGTH- neomycin, polymyxin b, pramoxine hcl cream
- NDC Code(s): 11822-0637-1, 11822-0637-2
- Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 21, 2024
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- 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 ingredients
- 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 cream
neomycin sulfate ● polymyxin B sulfate ● pramoxine HCl
first aid antibiotic/pain relieving cream
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 PLUS PAIN RELIEF MAXIMUM STRENGTH
neomycin, polymyxin b, pramoxine hcl creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-0637 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN 3.5 mg in 1 g PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE 10 mg in 1 g POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B 10000 [USP'U] in 1 g Inactive Ingredients Ingredient Name Strength METHYLPARABEN (UNII: A2I8C7HI9T) MINERAL OIL (UNII: T5L8T28FGP) POLOXAMER 188 (UNII: LQA7B6G8JG) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) PETROLATUM (UNII: 4T6H12BN9U) Product Characteristics Color WHITE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-0637-1 1 in 1 CARTON 07/14/2005 04/30/2025 1 14 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:11822-0637-2 1 in 1 CARTON 10/03/2018 06/30/2024 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 Drug M004 07/14/2005 04/30/2025 Labeler - Rite Aid Corporation (014578892)