Youth Dew Roll-on Antiperspirant Deodorant Liquid
FDA Label NDC 11559-001

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Estee Lauder Inc for the product Youth Dew Roll-on Antiperspirant Deodorant (NDC 11559-001). 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 otc - active ingredient, otc - purpose, warnings, otc - keep out of reach of children, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

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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