Ammens Medicated Powder Original

Manufacturer: Idelle Labs, Ltd | M.K. Packaging, Inc.
Effective date: 2017-12-29
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:53:53

Label at a glance#

ProductAmmens Medicated Powder Original

Active ingredientZINC OXIDE

Label structure11 sections

Dosage and administration

Apply as needed

Contacts and useful links#

PhoneLabel contact1-800-487-7273

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 5%

Purpose

OTC - PURPOSE SECTION

Skin Protectant

Use

INDICATIONS & USAGE SECTION

dries the oozing and weeping of poison:

• ivy

• oak

• sumac

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

• do not get into eyes

Stop use and ask doctor, if

OTC - STOP USE SECTION

• condition worsens

• symptoms last more than 7 days or clear up and occur again within a few days

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply as needed

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Zea Mays (Corn) Starch, Tricalcium Phosphate, Fragrance

Questions?

OTC - QUESTIONS SECTION

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)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1994530	Ammens 5 % Topical Powder	PSN	1
1994528	zinc oxide 0.05 MG/MG Topical Powder	PSN	1
1994530	zinc oxide 0.05 MG/MG Topical Powder [Ammens]	SBD	1
1994528	zinc oxide 0.05 MG/MG Topical Powder	SCD	1
1994530	Ammens 0.05 MG/MG Topical Powder	SY	1
1994528	zinc oxide 0.05 MG/MG Topical Powder	SY	1
1994528	ZNO 0.05 MG/MG Topical Powder	SY	1
1994530	ZNO 0.05 MG/MG Topical Powder [Ammens]	SY	1

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
ZINC CATION Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
f47a510b-6679-4664-b2d6-47b5c4afe7cc	Product name	4	20260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61c	Product name	2	20250515
0306390c-dd77-4363-afe0-63c58088b2a1	Product name	1	20220120
503ea967-4b9c-48cf-9e87-c7975295849d	Product name	2	20220120
190f2a5b-bbc8-65c7-fcb0-97891307b917	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
41595-1060-1	2022-01-28	C162847	48780-1	d6a99b39-82ba-a426-e053-dadaa90af4c2	AMMENS ® MEDICATED POWDER - ORIGINAL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
41595-1060-1	Ammens Medicated Powder Original	311 g in 1 CANISTER	POWDER	311		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
41595-1060	AMMENS MEDICATED POWDER ORIGINAL (ZINC OXIDE) POWDER [IDELLE LABS, LTD]	1	Legacy NDC, 1 package rows	20171231_44ec8ca9-4110-48f2-b519-3dda84a05ad1.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

Ammens Medicated Powder Original
Zinc Oxide
ZINC CATION
STARCH, CORN
TRICALCIUM PHOSPHATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
41595-1060	41595-1060-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ZINC OXIDE	SOI2LOH54Z	ACTIM
STARCH, CORN	O8232NY3SJ	IACT
TRICALCIUM PHOSPHATE	K4C08XP666	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
f3d37460-d4cb-4bc2-a3b2-18ed3091a3d0			44ec8ca9-4110-48f2-b519-3dda84a05ad1	2017-12-29	Warnings	Exact identifier spl id: f3d37460-d4cb-4bc2-a3b2-18ed3091a3d0 spl set id: 44ec8ca9-4110-48f2-b519-3dda84a05ad1

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.