Active Ingredient(S)
Aluminum Chlorohydrate 12.0%
Lumiste Desert Bloom
FDA Label NDC 87093-113
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Coco Cosmetics Inc for the product Lumiste Desert Bloom (NDC 87093-113). 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 active ingredient(s), purpose, use, warnings, otc - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiperspirant
Use
Reduces underarm wetness
48-hour protection
Warnings
For external use only.
Do not use on damaged skin.
Stop use if rash or irritation occurs
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
• Apply to underarms only
• Use on clean, dry skin
• Let dry before dressing
Other Information
• Protect from excessive heat and direct sunlight
• Store at 20-250C (68-770F)
• See bottom of packaging for lot number and expiration date
Inactive Ingredients
Aqua, Dicaprylyl Carbonate, Steareth-2, Parfum, Steareth-21, Dimethicone, 2-Methyl, 5-Cyclohexylpentanol, Amyl Cinnamal, Benzyl Salicylate, Citronellol, Hexyl Cinnamal, Limonene, Linalool, Acetyl Cedrene, Citrus Aurantium Peel Oil, Citrus Limon Peel Oil, Dimethyl Phenethyl Acetate, Linalyl Acetate, Pinene, Rose Ketones, Terpineol, Tetramethyl Acetylcyclohexenones
* Please review the disclaimer below.
