Label: MAXIM HYDROGEN PEROXIDE- hydrogen peroxide liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 69950-005-02 - Packager: Ostl, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 May 22, 2016
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- Drug Facts
- Active ingredients
- Purpose
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- INDICATIONS & USAGE
- Warnings
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- STORAGE AND HANDLING
- SPL UNCLASSIFIED SECTION
- Packaging
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INGREDIENTS AND APPEARANCE
MAXIM HYDROGEN PEROXIDE
hydrogen peroxide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69950-005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) HYDROGEN PEROXIDE 30 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PHOSPHORIC ACID (UNII: E4GA8884NN) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69950-005-02 295 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/17/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/17/2016 Labeler - Ostl, Inc. (020117798)