Active Ingredient
Zinc Oxide 5%
Ammens Medicated Powder Original
FDA Label NDC 41595-1060
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Idelle Labs, Ltd for the product Ammens Medicated Powder Original (NDC 41595-1060). 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, when using this product, stop use and ask doctor, if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Skin Protectant
Use
dries the oozing and weeping of poison:
• ivy
• oak
• sumac
Warnings
For external use only.
When Using This Product
• do not get into eyes
Stop Use And Ask Doctor, If
• condition worsens
• symptoms last more than 7 days or clear up and occur again within a few days
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Apply as needed
Inactive Ingredients:
Zea Mays (Corn) Starch, Tricalcium Phosphate, Fragrance
Questions?
call to 1-800-487-7273
©IDELLE LABS, LTD.
All rights reserved.
Distributed by Idelle Labs,
Ltd., El Paso, TX 79912
Ammens® is a trademark
of Kaz Europe Sarl.
Package Label.Principal Display Panel
AMMENS®
NEW 100% TALC FREE
TRUSTED FOR MORE THAN 100 YEARS
MEDICATED POWDER
ORIGINAL
Soothes
Relieves
Absorbs
Net Wt 11oz (311g)
Principal Display Panel (Ammens Medicated Powder 1)
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