Warnings
Please keep out of reach of children.
Deodorantantiperspirantspray
FDA Label NDC 84019-022
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shengnan (guangzhou) Cosmetics Co., Ltd for the product Deodorantantiperspirantspray (NDC 84019-022). 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 warnings, otc - purpose, otc - stop use, otc - active ingredient, otc - when using, inactive ingredient, dosage & administration, indications & usage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Reduces sweat production and keeps skin dry. While inhibiting sweat, it also prevents odor, ensuring a fresh body scent.
Otc - Stop Use
Discontinue use if skin shows abnormalreactions.A patch test on a small areaof skin is recommended before full use.
Otc - Active Ingredient
Aluminum Chlorohydrate
Otc - When Using
Please keep your skin dry before use to ensure the best results fromthe product.
Inactive Ingredient
Butylene Glycol
Propylene Glycol
Alcohol
Water
Fragrance
Algin
Agar
Titanium Dioxide
Pentylene Glycol
Polyoxyethylene Cetyl Stearyl Diether
Stearic Acid
C12-16 Alcohols
Phenoxyethanol
Menthol
Salvia Miltiorrhiza Root Extract
Eugenia Caryophyllus (Clove) Bud Extract
Angelica Polymorpha Sinensis Root Extract
Centella Asiatica Extract
Glycyrrhiza Uralensis (Licorice) Root Extract
Jojoba Esters
CI 26100
Dosage & Administration
Apply 2 times a day
Indications & Usage
Hold the bottle about 15 cm away fromthe underarm and spray evenly ontoclean, dry skin.
Package Label.Principal Display Panel
12 (3412312)
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