Label: NEOSPORIN PLUS LIDOCAINE- bacitracin, neomycin, polymyxin b, lidocaine ointment
- NDC Code(s): 69968-0731-1
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 15, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
-
Warnings
For external use only
Do not use
- if you are allergic to any of the ingredients
- in the eyes
- over large areas of the body
- in large quantities, particularly over raw surfaces or blistered areas
- Directions
- Other information
- Inactive ingredient
- Questions?
- SPL UNCLASSIFIED SECTION
-
PRINCIPAL DISPLAY PANEL - 14.2 g Tube Carton
#1
DOCTOR
RECOMMENDED
BRAND
NEOSPORIN®
+ MAXIMUM STRENGTH
LIDOCAINE
With Fast-Acting Lidocaine
For Pain Relief*
Numbs Away the Pain
24-Hour Infection
Protection
NUMBING
OINTMENT
FIRST AID ANTIBIOTIC / PAIN RELIEVING OINTMENT
Bacitracin Zinc – Lidocaine – Neomycin Sulfate – Polymyxin
B Sulfate
NET WT. 0.5 OZ (14.2 g)
-
INGREDIENTS AND APPEARANCE
NEOSPORIN PLUS LIDOCAINE
bacitracin, neomycin, polymyxin b, lidocaine ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0731 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 40 mg in 1 g BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 500 [iU] in 1 g NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg in 1 g POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B 10000 [iU] in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0731-1 1 in 1 CARTON 01/30/2023 1 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 01/30/2023 Labeler - Kenvue Brands LLC (118772437)