Active Ingredient
Aluminum Sesquichlorohydrate 17.6%
The following Structured Product Label (SPL) was submitted to the FDA by Lume Deodorant, Llc. for the product Lume Deodorant With Clinical Strength Sweat Control, Soft Powder (NDC 84520-034). 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, purpose, use, warnings, keep out of reach of children, directions, inactive ingredients, lume whole body deodorant plus sweat control smooth solid, unscented, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Aluminum Sesquichlorohydrate 17.6%
Antiperspirant
For external use only
Do not use on broken or irritated skin
Ask a doctor before use if you have kidney disease
Stop use if rash or irritation occurs
Sunburn Alert: This product contains an alpha hydroxy acid (AHA) that may increase your skin’s sensitivity to the sun and particularly the possibility of sunburn. Use a sunscreen, wear protective clothing, and limit sun exposure while using this product for a week afterwards.
KEEP OUT OF REACH OF CHILDREN
PPG-15 Stearyl Ether, Ozokerite, Neopentyl Glycol Diheptanoate, Stearyl Alcohol, Isododecane, Isopentyldiol, Lauryl Laurate, Mandelic Acid, Sorbitan Oleate, Fragrance (Parfum), Maranta Arundinacea Root Powder, Silica, Citronellyl Methylcrotonate, Zea Mays (Corn) Starch, Panthenol, Caffeine, Ethylhexylglycerin.
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