Label: HYDROGEN PEROXIDE solution
- NDC Code(s): 49035-871-43, 49035-871-45, 49035-871-99
- Packager: Wal-Mart Stores, Inc.
- Category: HUMAN OTC DRUG LABEL
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 March 22, 2022
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- Do not use
- Ask a doctor before use if you have
- Stop use and ask a doctor if
- Keep out of reach of children.
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Directions
For First aid:
- clean the affected area
- spray 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: adults, children over 2 years of age:
- mix with an equal amount of water
- swish around in the mouth over the affected area for at least 1 minute, then spit out
- use up to 4 times daily after meals and at bedtime
- children under 12 years of age should be supervised in the use
- children 2 years of age: consult a dentist, doctor
- Other information
- Inactive ingredients
- SPL UNCLASSIFIED SECTION
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principal display panel
Do not use if printed seal under cap is broken or missing
NDC 49035-871-43
Hydrogen Peroxide Topical Solution USP
first aid antiseptic
oral debriding agentMade in the USA factory Certified
Use for:
- For treatment of minor cuts and abrasions
- For use as a gargle or rinse
Square bottles use less plastic than a similarly sized round bottle
Recyclable (if available in your area)
16 FL OZ (1 PT) 473 mL
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INGREDIENTS AND APPEARANCE
HYDROGEN PEROXIDE
hydrogen peroxide solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-871 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) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-871-99 236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/08/2019 2 NDC:49035-871-43 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/09/2017 3 NDC:49035-871-45 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/09/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/09/2017 Labeler - Wal-Mart Stores, Inc. (051957769) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(49035-871) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(49035-871)