Label: HYDROGEN PEROXIDE solution
- NDC Code(s): 68599-2301-2, 68599-2301-6, 68599-2301-9
- Packager: McKesson Medical-Surgical Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 15, 2024
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- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Uses
- Warnings
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Directions
First aid antiseptic:
- Clean the affected area
- Apply a small amount of product on the area 1 to 3 times daily
- 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 or doctor
- 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
- SPL UNCLASSIFIED SECTION
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PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label
NDC 68599-2301-6
McKESSON
Hydrogen
Peroxide 3%TOPICAL SOLUTION USP
FIRST AID ANTISEPTIC
ORAL DEBRIDING AGENTFor treatment of minor cuts and abrasions.
For use as a gargle or rinse. Tamper evident cap
for your protection. If ring-band is detached from
cap or missing, do not use.16FL OZ (1 pt)
(473 mL)MFR # 23-D0012
Distributed By McKesson Medical-Surgical Inc.
Richmond, VA 23233
LU-5750-1112 1-07-D0012R10
Made in USA - PRINCIPAL DISPLAY PANEL - 473 mL Drug facts panel
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
HYDROGEN PEROXIDE
hydrogen peroxide solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68599-2301 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:68599-2301-2 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/09/2013 2 NDC:68599-2301-6 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/09/2013 3 NDC:68599-2301-9 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/09/2013 09/02/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 10/09/2013 Labeler - McKesson Medical-Surgical Inc. (023904428)