HYDROGEN PEROXIDE liquid

HYDROGEN PEROXIDE by

Drug Labeling and Warnings

HYDROGEN PEROXIDE by is a Otc medication manufactured, distributed, or labeled by Medical Chemical Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Usage: Intended for use as a general purpose topical antiseptic for first-aid treatment of minor cuts and abrasions.  In case of deep or puncture wounds consult a physician.  Discontinue use and get medical attention if redness, irritation or infection develops.

ACTIVE INGREDIENT

Active ingredient: hydrogen peroxide, 3% w/v in water.

KEEP OUT OF REACH OF CHILDREN

For External Use Only.  Do not use in eyes or over large areas of the body.  Keep out of the reach of children.

INDICATIONS & USAGE

Usage: Intended for use as a general purpose topical antiseptic for first-aid treatment of minor cuts and abrasions.  In case of deep or puncture wounds consult a physician.  Discontinue use and get medical attention if redness, irritation or infection develops.

WARNINGS

For External Use Only.  Do not use in eyes or over large areas of the body.  Keep out of the reach of children.

DOSAGE & ADMINISTRATION

For oral hygiene, dilute with an equal volume of water and gargle for about one minute.  Rinse with water.  In case of accidental ingestion contact a physician or a poison control center.

INACTIVE INGREDIENT

Active ingredient: hydrogen peroxide, 3% w/v in water.

PRINCIPAL DISPLAY PANEL

h2o2label.jpg

INGREDIENTS AND APPEARANCE

HYDROGEN PEROXIDE 
hydrogen peroxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 12745-202
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V)	HYDROGEN PEROXIDE	8.57 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 12745-202-01	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/21/1980
2	NDC: 12745-202-02	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/21/1980
3	NDC: 12745-202-03	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/21/1980

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/21/1980

Labeler - Medical Chemical Corporation (008496861)

Establishment
Name	Address	ID/FEI	Business Operations
Medical Chemical Corporation		008496861	manufacture(12745-202)