Label: NEOSPORIN PAIN ITCH SCAR- bacitracin zinc, neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride ointment
- NDC Code(s): 69968-0093-1, 69968-0093-2
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 13, 2024
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- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
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- SPL UNCLASSIFIED SECTION
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PRINCIPAL DISPLAY PANEL - 28.3 g Tube Carton
#1 DOCTOR
RECOMMENDED
BRAND
NEOSPORIN ®
+
PAIN + ITCH + SCARMaximum Strength:
Infection Protection,
Pain and Itch Relief24-Hour Infection
ProtectionMinimizes the
Appearance
of ScarsNO STING
OINTMENT
FIRST AID ANTIBIOTIC/PAIN RELIEVING OINTMENT
Bacitracin Zinc - Neomycin Sulfate - Polymyxin B Sulfate –
Pramoxine HClNET WT 1.0 OZ (28.3 g)
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INGREDIENTS AND APPEARANCE
NEOSPORIN PAIN ITCH SCAR
bacitracin zinc, neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0093 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 500 [iU] 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 [iU] in 1 g PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE 10 mg in 1 g Inactive Ingredients Ingredient Name Strength LEVANT COTTONSEED OIL (UNII: N5CFT140R8) OLIVE OIL (UNII: 6UYK2W1W1E) COCOA BUTTER (UNII: 512OYT1CRR) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PETROLATUM (UNII: 4T6H12BN9U) SODIUM PYRUVATE (UNII: POD38AIF08) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0093-1 1 in 1 CARTON 01/15/2016 1 28.3 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:69968-0093-2 1 in 1 CARTON 01/15/2016 2 14.2 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 01/15/2016 Labeler - Kenvue Brands LLC (118772437)