HYDROGEN PEROXIDE- hydrogen peroxide liquid 
Medical Chemical Corporation

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.

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Hydrogen Peroxide 3% Label

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

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

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.

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

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.

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

h2o2label.jpg

Hydrogen Peroxide Label

HYDROGEN PEROXIDE 
hydrogen peroxide liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12745-202
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) HYDROGEN PEROXIDE8.57 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:12745-202-0159 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/21/1980
2NDC:12745-202-02118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/21/1980
3NDC:12745-202-033785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/21/1980
4NDC:12745-202-04208175 mL in 1 DRUM; Type 0: Not a Combination Product07/21/1980
5NDC:12745-202-05946250 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product07/21/1980
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/21/1980
Labeler - Medical Chemical Corporation (008496861)
Establishment
NameAddressID/FEIBusiness Operations
Medical Chemical Corporation008496861manufacture(12745-202)

Revised: 1/2022
Document Id: d5d0f666-62c0-438e-e053-2a95a90a8db2
Set id: f6d677b8-fa89-4efb-984a-fd98e3e590e8
Version: 17
Effective Time: 20220117
 
Medical Chemical Corporation