Active Ingredient
Aluminum Chlorohydrate 20%
Clarisse Antiperspirant Deodoranrt Cherry Blossom Stick
FDA Label NDC 76176-016
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Liyuan Daily Chemical Products Co., Ltd. for the product Clarisse Antiperspirant Deodoranrt Cherry Blossom (NDC 76176-016). 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, do not use, ask a doctor before use, stop use and ask a doctor, keep out of reach of children., 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
Warnings
For external use only
Do Not Use
on broken or irritated skin
Ask A Doctor Before Use
if you have kidney disease
Stop Use And Ask A Doctor
if irritation or rash develops
Keep Out Of Reach Of Children.
If swallowed, seek medical help or contact a Poison Control Center immediately.
Directions
apply to underarms only
Inactive Ingredients
mineral oil, stearic acid, stearyl alcohol, zea mays (corn) starch, zinc palmitate, cyclopentasiloxane, hydrogenated castor oil, fragrance, PPG-14 butyl ether, PEG-8 distearate, butylated hydroxytoluene
Package Label.Principal Display Panel
Label (8913)
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