Label: HYDROGEN PEROXIDE solution
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NDC Code(s):
72476-942-34,
72476-942-43,
72476-942-45,
72476-942-50, view more72476-942-72, 72476-942-99
- Packager: Retail Bsiness Services, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 6, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
- 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
First Aid Antiseptic:
- clean the affected area
- apply a small amount of the product on the affected area 1 to 3 times a day
- may be covered with a sterile bandage
- if bandage, let dry first
Oral Debriding Agent:
- adults, children over 2 years of age
- mix with 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 under 2 years of age: consult a dentist or doctor
- Other information
- Inactive ingredient
- principal display panel
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INGREDIENTS AND APPEARANCE
HYDROGEN PEROXIDE
hydrogen peroxide solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72476-942 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:72476-942-34 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/10/2011 2 NDC:72476-942-43 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/10/2011 3 NDC:72476-942-50 710 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/10/2011 4 NDC:72476-942-45 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/10/2011 5 NDC:72476-942-99 236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 12/10/2011 6 NDC:72476-942-72 296 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 12/10/2011 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 12/10/2011 Labeler - Retail Bsiness Services, LLC (967989935) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(72476-942)