Otc - Purpose
Use: Reduces underarm perspiration.
Anti-perspirant Deodorant
FDA Label NDC 57367-008
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by 220 Laboratories Inc for the product Anti-perspirant Deodorant (NDC 57367-008). 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 - purpose, dosage & administration, warnings, otc - active ingredient, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Dosage & Administration
Directions: Apply to underarms only.
Warnings
Warnings: For external use only. Keep out of reach of children.
Otc - Active Ingredient
Active Ingredients: Aluminum Chlorohydrate 5.2%.
Inactive Ingredient
Inactive Ingredients: Propylene Glycol, Purified Water, Sodium Stearate, Steareth-20, Fragrance, Sodium Hydroxide.
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