Otc - Active Ingredient
Hydrogen Peroxide 2.80%
White Labs
FDA Label NDC 73660-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bs And Co. Ltd for the product White Labs (NDC 73660-001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, indications & usage, dosage & administration, warnings, otc - ask doctor, otc - keep out of reach of children, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Oral Debriding
Indications & Usage
Aids in the removal of phlegm, mucus, or other secretions associated with occasional sore mouth
Dosage & Administration
Use up to 2 times daily after meals and at bedtime
children under 13 years of age Do not use
Warnings
For external use only
Otc - Ask Doctor
The condition persists or gets worse
Sore mouth symptoms do not improve in 7 days
Irritation, pain or redness persists or worsens
Swelling, rash or fever develops
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away
Inactive Ingredient
Distilated water, Polyvinyl alcohol, Titanium dioxide, Poloxamer 407, Glycerine, PEG400, Ethanol, PVP K29/32(Povidone), PVP K90(Povidone), Aerosil 200, Flavor(Applemint HF62184), Citric Acid, Sodium Citric Acid
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