Other
Drug Facts
Manufactured for:
CHARM-TEX, INC.
1618 Coney Island Ave., Brooklyn NY 11230
Charm-tex
FDA Label NDC 40057-6001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Charm-tex, Inc for the product Charm-tex (NDC 40057-6001). 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 other, active ingredient, purpose, use, warnings, otc - do not use, otc - stop use, otc - ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Aluminum Zirconium Tetrachlorohydrex Gly 0.3%
Purpose
Antiperspirant
Use
Reduces underarm perspiration
Warnings
For external use only.
Otc - Do Not Use
Do not use on broken skin.
Otc - Stop Use
Stop use if rash or irritation occurs. If condition persists for more than 72 hours consult a doctor.
Otc - Ask Doctor
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 and contact Poison Control Center right away.
Directions
Apply to underarms only.
Inactive Ingredients
Water, Glyceryl Stearate, Peg 100 Stearate, Magnesium, Aluminum, Silicate, Fragrance
Principal Display Panel - 44 Ml Label
Charm-Tex
ANTIPERSPIRANT
ROLL-ON
DEODORANT
ALCOHOL FREE
Net Wt. 1.5 oz. 44 ml.
Principal Display Panel (44 ml label)
* Please review the disclaimer below.
