FDA Label for Youth Dew Roll-on Antiperspirant Deodorant
View Indications, Usage & Precautions
Youth Dew Roll-on Antiperspirant Deodorant Product Label
The following document was submitted to the FDA by the labeler of this product Estee Lauder Inc. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - Active Ingredient
ACTIVE INGREDIENT:ALUMINUM CHLOROHYDRATE 20.00%
Otc - Purpose
USES: DECREASES UNDERARM PERSPIRATION
Warnings
WARNINGS:
- FOR EXTERNAL USE ONLY
- DO NOT USE ON BROKEN SKIN
- STOP USE IF RASH OR IRRITATION OCCURS
- ASK A DOCTOR BEFORE USE IF YOU HAVE KIDNEY DISEASE
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.
Dosage & Administration
DIRECTIONS: APPLY TO UNDERARMS ONLY
Inactive Ingredient
INACTIVE INGREDIENTS: WATER [] STEARETH-2 [] ALCOHOL DENAT. [] PPG-11 STEARYL ETHER [] STEARETH-20 [] YOUTH-DEW FRAGRANCE (PARFUM) [] MYRISTALKONIUM CHLORIDE [] QUATERNIUM-14 []TRISODIUM EDTA [] SORBIC ACID ILN32521
Package Label.Principal Display Panel
PRINCIPAL DISPLAY PANEL:
YOUTH-DEW
ROLL-ON
ANTI-PERSPIRANT
DEODORANT
ACTIVE INGREDIENT: ALUMINUM CHLOROHYDRATE 20.00%
2.5 FL OZ LIQ/ 75 mL
ESTEE LAUDER DIST
NY, NY 10022
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