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: Johnson & Johnson Consumer Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 11, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
- Warnings
- Directions
- Other information
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
-
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)
-
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 PETROLATUM (UNII: 4T6H12BN9U) LEVANT COTTONSEED OIL (UNII: N5CFT140R8) OLIVE OIL (UNII: 6UYK2W1W1E) COCOA BUTTER (UNII: 512OYT1CRR) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) 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 final part333B 01/15/2016 Labeler - Johnson & Johnson Consumer Inc. (118772437)