Active Ingredients
Propylene Glycol 5%
Antiperspirant Deodorant
FDA Label NDC 83566-567
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Yilong Cosmetics Co., Ltd for the product Antiperspirant Deodorant (NDC 83566-567). 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 ingredients, purpose, uses, warning, stop use and ask a doctor if, do not use, when using this product, 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 fragrance
Uses
STEP1: Clean and thoroughly dry your skin.
STEP2: Twist the bottom of the product.
STEP3: Gently apply to the underarms or other desired areas.
Warning
For external use only
Stop Use And Ask A Doctor If
rash occurs
Do Not Use
on damaged or broken skin
When Using This Product
keep out of eyes,rinse with water to remove
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Inactive Ingredient
Water 60%
Stearic Acid 4%
Sodium Hydroxide 3%
Polysorbate 20 2%
Polysorbate 60 2%
Sucrose 2%
Tetrasodium EDTA 1%
Parfum 1%
Saururus Chinensis Leaf/Root Extract 0.4%
Taraxacum Officinale (Dandelion) Leaf Extract 0.37%
Stephania Tetrandra Root Extract 0.14% Cl 42090 0.08%
Cl 17200 0.01%
Dosage & Administration
Squeeze out an appropriate amount of sunscreen and spread evenly on skin,
Package Label.Principal Display Panel
Label (01)
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