Jafra Daily
FDA Label NDC 68828-052

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Jafra Cosmetics International for the product Jafra Daily (NDC 68828-052). 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, inactive ingredient, indications & usage, dosage & administration, warnings, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

ACTIVE INGREDIENTALUMINUM ZIRCONIUMTETRACHLOROHYDRATEGLYCINE COMPLEX 15%

Otc - Purpose

PURPOSE

ANTIPERSPIRANT

Inactive Ingredient

INACTIVE INGREDIENTS: WATER/AQUA, CYCLOMETHICONE, PPG-15 STEARYL ETHER, STEARETH-2, CETETH-20, FARNESOL, AVENA SATIVA (OAT) KERNEL EXTRACT, FRAGRANCE/PARFUM, ISOPROPYL PALMITATE, TRICONTANYL PVP, BUTYLENE GLYCOL, PHENOXYETHANOL, METHYLPARABEN, ETHYLPARABEN, PROPYLPARABEN, BUTYLPARABEN.

Indications & Usage

USES

  • REDUCES UNDERARM WETNESS

Dosage & Administration

DIRECTIONS

  • APPLY TO UNDERARMS ONLY

Warnings

WARNINGS

  • DO NOT USE ON BROKEN SKIN.

Otc - Stop Use

  • STOP USE IF RASH OR IRRITATION OCCURS.

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.

Package Label.Principal Display Panel

JAFRA

DAILY
FLORAL MIST
FOR WOMEN
ANTIPERSPIRANT
DEODORANT ROLL-ON

60 G / NET WT 2 OZ

Otc - Ask Doctor

  • ASK A DOCTOR BEFORE USE IF YOU HAVE KIDNEY DISEASE.

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