Label: HYDROGEN PEROXIDE liquid
- NDC Code(s): 70000-0022-1, 70000-0022-3
- Packager: Cardinal Health, 110 dba Leader
- 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 April 13, 2022
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- Active Ingredient
- Uses
- Warnings
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Directions
First aid antiseptic
- clean the affected area
- apply a small amount of product on the affected area 1 to 3 times a day
- may be covered with a sterile bandage
- if bandaged, let dry first
Oral debriding agent (oral rinse): adults and children 2 years of age and over:
- mix with an equal amount of water
- swish around in the mouth over the affected area for at least 1 minute and then spit out
- use up to 4 times daily after meals and at bedtime or as directed by a dentist
- children under 12 years of age should be supervised in the use of this product
- children under 2 years of age: consult a dentist or doctor
- Other information
- Inactive ingredient
- questions
- Adverse Reactions
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NDC 70000-0022-1
Hydrogen Peroxide
Topical Solution USP, 3%
First Aid Antiseptic
Oral Debriding Agent
DO NOT USE IF PRINTED SEAL UNDER CAP IS BROKEN OR MISSING.
Drug Facts
Active ingredent Purpose
Hydrogen peroxide (stablized) 3%----------First aid antiseptic, Oral debriding agent
Pat. D675,101
100% Money Back Guarantee Return to place of purchase if not satisfied.
Dist. by CAH, Dublin, OH 43017
2019 Cardinal Health
CIN 5516075 REV 6/19
8 FL OZ (236 mL)
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INGREDIENTS AND APPEARANCE
HYDROGEN PEROXIDE
hydrogen peroxide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70000-0022 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) HYDROGEN PEROXIDE 3 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70000-0022-1 236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/19/2019 2 NDC:70000-0022-3 236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/19/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/19/2019 Labeler - Cardinal Health, 110 dba Leader (063997360) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(70000-0022) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(70000-0022)