Clinical Strength Miracledry Antiperspirant Deodorant Am Liquid
FDA Label NDC 53897-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Highland Consumer Products for the product Clinical Strength Miracledry Antiperspirant Deodorant Am (NDC 53897-000). 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 drug facts, active ingredient, otc - purpose, uses, warnings, do not use, keep out of reach of children, stop use and contact a 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 Octachlorohydrex Gly Anhydrous 18%
Otc - Purpose
Antiperspirant
Uses
Treats excessive perspiration and reduces underarm wetness and odor.
Warnings
For external use only
Do Not Use
on irritated skin.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away
Stop Use And Contact A Doctor
if rash or irritation develops
Ask Your Doctor
before using if you have kidney disease
Directions
Apply to underarms only. Use in the morning every day. Apply few strokes to underarms after tipping bottle to get maximum effect.
Inactive Ingredients
Water, PPG-11 Stearyl Ether, Cyclopentasiloxane, Steareth-2, Steareth-20, Isopropyl Myristate, Glycine, Steareth-21
Storage
Keep at room temperature
Questions?
www.miracledry.com
Package Label.Principal Display Panel
clinical strength Miracle Dry ANTIPERSPIRANT DEODORANT AM day formula 1.7 FL OZ 50.3 ML
Product Label
Miracle Dry Am (Miracledryam)
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