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NDC 69842-0610-71 CVS Triple Antibiotic 400; 3.5; 5000 [USP'U]/g; mg/g; [USP'U]/g Details

CVS Triple Antibiotic 400; 3.5; 5000 [USP'U]/g; mg/g; [USP'U]/g

CVS Triple Antibiotic is a TOPICAL OINTMENT in the HUMAN OTC DRUG category. It is labeled and distributed by CVS Pharmacy. The primary component is BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE.

MedlinePlus Drug Summary

Neomycin, polymyxin, and bacitracin combination is used to prevent minor skin injuries such as cuts, scrapes, and burns from becoming infected. Neomycin, polymyxin, and bacitracin are in a class of medications called antibiotics. Neomycin, polymyxin, and bacitracin combination works by stopping the growth of bacteria.

Related Packages: 69842-0610-71
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Neomycin, Polymyxin, and Bacitracin Topical

Product Information

NDC	69842-0610
Product ID	69842-610_45d5e475-0982-038e-e054-00144ff88e88
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	CVS Triple Antibiotic
Proprietary Name Suffix	n/a
Non-Proprietary Name	Bacitracin, Neomycin, Polymyxin B
Product Type	HUMAN OTC DRUG
Dosage Form	OINTMENT
Route	TOPICAL
Active Ingredient Strength	400; 3.5; 5000
Active Ingredient Units	[USP'U]/g; mg/g; [USP'U]/g
Substance Name	BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Labeler Name	CVS Pharmacy
Pharmaceutical Class	Aminoglycoside Antibacterial [EPC], Aminoglycosides [CS], Decreased Cell Wall Synthesis & Repair [PE], Polymyxin-class Antibacterial [EPC], Polymyxins [CS]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part333B
Listing Certified Through	2024-12-31

Package

Package Images

NDC 69842-0610-71 (69842061071)

Pricing Information	N/A
NDC Package Code	69842-610-71
Billing NDC	69842061071
Package	1 BOTTLE in 1 PACKAGE (69842-610-71) / 7.7 g in 1 BOTTLE
Marketing Start Date	2008-11-01
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 454bfeed-f58f-003a-e054-00144ff8d46c Details

Drug Facts

Active Ingredients (in each gram)

Bacitracin 400 units

Neomycin 3.5 mg

Polymyxin B 5,000 units

Uses

first aid to help prevent infection in minor:

• cuts • scrapes • burns

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

Ask a doctor before use if you have

• deep or puncture wounds • animal bites • serious burns

Stop use and ask a doctor if

• you need to use longer than 1 week

• condition persists or gets worse

• rash or other allergic reaction develops • side effects occur. You may report side effects to FDA at 1-800-FDA-1088.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• clean the affected area • apply a small amount of product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily • may be covered with a sterile bandage

Inactive Ingredients

white petrolatum

Purpose

First Aid Antibiotic

Other information

•store at controlled room temperature

• prior to initial use, please prime pump by depressing multiple times

Questions or Comments?

1-800-635-3696

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CVS TRIPLE ANTIBIOTIC

bacitracin, neomycin, polymyxin b ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69842-610
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN	400 [USP'U] 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	5000 [USP'U] in 1 g

Ingredient Name	Strength
Inactive Ingredients
PETROLATUM (UNII: 4T6H12BN9U)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:69842-610-71	1 in 1 PACKAGE	11/01/2008
1		7.7 g in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333B	11/01/2008

Labeler - CVS Pharmacy (062312574)

Revised: 1/2017

Document Id: 45d5e475-0982-038e-e054-00144ff88e88

Set id: 454bfeed-f58f-003a-e054-00144ff8d46c

Version: 5

Effective Time: 20170104