Active Ingredient
Aluminum Zirconium Trichlorohydrex GLY 20%
Mossy Oak Eclipse
FDA Label NDC 10889-427
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Vvf Kansas Services Llc for the product Mossy Oak Eclipse (NDC 10889-427). 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 active ingredient, purpose, use, warnings, otc - do not use, otc - stop use, otc - ask doctor, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiperspirant
Use
- reduces underarm wetness
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.
Otc - Ask Doctor
Ask a doctor before use if you have kidney disease.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Apply to underarms only
Inactive Ingredients
Cyclopentasiloxane, Stearyl Alcohol, PPG-14
Butyl Ether, Hydrogenated Castor Oil, Mineral Oil,
Glyceryl Stearate, PEG-100 Stearate.
Questions?
Call 1-800-873-5873
Other
Mossy Oak Eclipse™ Antiperspirant & Deodorant
Manufactured for: Wildlife Research Center, Inc
14485 Azurite St. NW, Ramsey, MN 55303
UPC: 0-24641-80847-4
Packaging Copyright ©2019
Official License Product of Haas Outdoors, Inc. West Point,
MS 39773. Distributed by Wildlife Research Center, Inc.
14487 Azurite St NW, Ramsey, MN 55303
Mossy Oak is a trademark used under license from Haas
Outdoors, Inc. by Wildlife Research Center, Inc.
Mossy Oak Eclipse™
Antiperspirant & Deodorant
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NET WT 2.25 OZ (64 g)
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