BACITRACIN ZINC ointment

Bacitracin Zinc by

Drug Labeling and Warnings

Bacitracin Zinc by is a Otc medication manufactured, distributed, or labeled by Blossom Pharmaceuticals. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient                         Purpose
Bacitracin Zinc 500 Units                Antibiotic

Warnings:

For external use only

Dosage & Administration

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

Indications & Usage

• if you are allergic to any of the ingredients
• in the eyes
• over large areas of the body
• longer than 1 week unless directed by a doctor

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN
If swallowed, get medical help or contact a Poison Control Center right away

Purpose:

First aid to help prevent infection in:

• Minor cuts
• scrapes
• burns

Ask a doctor before use:

• in case of deep or puncture wounds
• animal bites
• serious burns
  

Other information

• store at controlled room temperature 15°-30° C (59°-86° F)

Stop Use and ask a doctor if

• the condition persists or gets worse, or if a rash or other allergic reaction develops.

Inactive ingredients

Hard Paraffin, Liquid Paraffin, White Soft Paraffin

Principal Display Panel

Blossom Pharmaceuticals Bacitracin Zinc Ointment:

bacitracin zinc.jpg

INGREDIENTS AND APPEARANCE

BACITRACIN ZINC 
bacitracin zinc ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61767-220
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN	500 [USP'U]  in 1 g

Inactive Ingredients
Ingredient Name	Strength
PETROLATUM (UNII: 4T6H12BN9U)
LIGHT MINERAL OIL (UNII: N6K5787QVP)
MINERAL OIL (UNII: T5L8T28FGP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61767-220-02	28.35 g in 1 TUBE
2	NDC: 61767-220-03	14.17 g in 1 TUBE
3	NDC: 61767-220-04	113.4 g in 1 TUBE
4	NDC: 61767-220-07	425.3 g in 1 JAR
5	NDC: 61767-220-05	0.5 g in 1 PACKET
6	NDC: 61767-220-01	0.9 g in 1 PACKET

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333B	05/14/2014

Labeler - Blossom Pharmaceuticals (677381470)

Establishment
Name	Address	ID/FEI	Business Operations
Blossom Pharmaceuticals		677381470	manufacture(61767-220)