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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