Ammens Medicated Powder Shower Fresh

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 22:53:54

Label at a glance#

ProductAmmens Medicated Powder Shower Fresh
Active ingredientZINC OXIDE
Label structure11 sections

Dosage and administration

Apply as needed

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, Aloe Barbadensis Leaf Extract

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

SHOWER FRESH with ALOE

Soothes

Relieves

Absorbs

Net Wt 11oz (311g)

ammenspowderdrugpanel
ammenspowderdrugpanel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1994530Ammens 5 % Topical PowderPSN1
1994528zinc oxide 0.05 MG/MG Topical PowderPSN1
1994530zinc oxide 0.05 MG/MG Topical Powder [Ammens]SBD1
1994528zinc oxide 0.05 MG/MG Topical PowderSCD1
1994530Ammens 0.05 MG/MG Topical PowderSY1
1994528zinc oxide 0.05 MG/MG Topical PowderSY1
1994528ZNO 0.05 MG/MG Topical PowderSY1
1994530ZNO 0.05 MG/MG Topical Powder [Ammens]SY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
41595-1061-12022-01-28C16284748780-1d6a99b39-82bd-a426-e053-dadaa90af4c2AMMENS ® MEDICATED POWDER - SHOWER FRESH

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41595-1061-1Ammens Medicated Powder Shower Fresh311 g in 1 CANISTERPOWDER3111

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41595-1061AMMENS MEDICATED POWDER SHOWER FRESH (ZINC OXIDE) POWDER [IDELLE LABS, LTD]1Legacy NDC, 1 package rows20171231_fc6db9f3-9059-40bb-84bf-69a3c0838bfa.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41595-106141595-1061-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
213a3fb4-d15a-4a72-aa92-dee7fa228356fc6db9f3-9059-40bb-84bf-69a3c0838bfa2017-12-29WarningsExact identifier
spl id: 213a3fb4-d15a-4a72-aa92-dee7fa228356
spl set id: fc6db9f3-9059-40bb-84bf-69a3c0838bfa

Reported adverse events (FAERS/openFDA)#

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