Antiperspirant Blush Lilly Aerosol, Spray
FDA Label NDC 52000-446
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Universal Distribution Center Llc for the product Antiperspirant Blush Lilly (NDC 52000-446). 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 drug facts, active ingredient, purpose, uses:, warnings, otc - keep out of reach of children, directions:, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Aluminum Chlorohydrate (23.3%)
Purpose
Antiperspirant
Uses:
Reduces underarm wetness.
Warnings
• FLAMMABLE. DO NOT USE NEAR HEAT, FLAME, OR WHILE SMOKING. CAN CAUSE SERIOUS INJURY OR DEATH.
• Keep away from face and mouth to avoid breathing in.
• Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate.
• Do not use on broken skin. Stop use if rash or irritation occurs.
• Ask a doctor before use if you have kidney disease.
Otc - Keep Out Of Reach Of Children
• KEEP OUT OF REACH OF CHILDREN.
• USE ONLY AS DIRECTED. INTENTIONAL MISUSE BY DELIBERATELY CONCENTRATING AND INHALING THE CONTENTS CAN BE HARMFUL OR FATAL.
Directions:
Apply to underarms only.
Inactive Ingredients
Cyclopentasiloxane, Butane, Propane, Isobutane, Hydrofluorocarbon 152A, PPG-14 Butyl Ether, C12-15 Alkyl Benzoate, Dimethiconol, Disteardimonium Hectorite, Helianthus Annuus (Sunflower) Seed Oil, Octyldodecanol, Fragrance (Parfum), BHT, Propylene Carbonate, Tocopheryl Acetate.
Packaging
Antiperspirant Blush Lilly (52000446 5)
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