Label: NEOSPORIN PLUS LIDOCAINE- bacitracin, neomycin, polymyxin b, lidocaine ointment
- NDC Code(s): 69968-0731-1
- 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 9, 2023
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- Download DRUG LABEL INFO: PDF XML
- 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 final part333B 01/30/2023 Labeler - Johnson & Johnson Consumer Inc. (118772437)