Quality Choice 063.001/063AA Calamine Lotion

Manufacturer: Chain Drug Marketing Association | Nice-Pak Products, LLC
Effective date: 2026-02-27
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 01:47:55

Label at a glance#

ProductCalamine

Active ingredientFERRIC OXIDE RED, ZINC OXIDE

Label structure12 sections

Dosage and administration

shake well before using apply as needed

Storage and handling

store at 59⁰ - 86⁰ F

Contacts and useful links#

PhoneLabel contact800-935-2362

Websitewww.qualitychoice.com

www.qualitychoice.com

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Calamine 8%
Zinc oxide 8%

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 a 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

shake well before using
apply as needed

Other information

STORAGE AND HANDLING SECTION

store at 59⁰ - 86⁰ F

Inactive ingredients

INACTIVE INGREDIENT SECTION

bentonite magma, calcium hydroxide, glycerin, purified water

ADVERSE REACTION

ADVERSE REACTIONS SECTION

Distributed by CMDA, Inc.

Novi, MI 48375

www.qualitychoice.com

Questions: 800-935-2362

SATISFACTION GUARANTEED

100% QC

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 83324-248-06

QUALITY CHOICE

Calamine

Lotion

Calamine Topical Suspension USP

Skin Protectant

Dries the Oozing and Weeping of Poison:

Ivy, Oak & Sumac

6 FL OZ (177 mL)

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
617954	calamine 8 % / zinc oxide 8 % Topical Lotion	PSN	3
617954	calamine 80 MG/ML / zinc oxide 80 MG/ML Topical Lotion	SCD	3
617954	calamine 8 % / zinc oxide 8 % Topical Lotion	SY	3
617954	Calamine 80 MG/ML / ZNO 80 MG/ML Topical Lotion	SY	3

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Data code	Data Matrix	L0022070SA		mm01.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
83324-248-06	Calamine	177 mL in 1 BOTTLE, PLASTIC	LOTION	177		3

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
83324-248-06	ML - Milliliter	83324-248	1d8abc00-d25a-45d7-a3cf-3d921ffc987b	1	2025-05-14

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Calamine
FERRIC OXIDE RED
BENTONITE
CALCIUM HYDROXIDE
GLYCERIN
WATER
ZINC OXIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
83324-248	83324-248-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENTONITE	A3N5ZCN45C	IACT
CALCIUM HYDROXIDE	PF5DZW74VN	IACT
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT
FERRIC OXIDE RED	1K09F3G675	ACTIB
ZINC OXIDE	SOI2LOH54Z	ACTIB

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
Calamine	FERRIC OXIDE RED	Chain Drug Marketing Association	86ff4875-9007-4b7b-8f46-16cbd475d4bb	2026-02-27	Warnings, Adverse reactions	Exact identifier ndc (package): 83324-248-06 ndc (product): 83324-248 ndc11 (package): 83324024806 spl id: 4bcf3ffc-3e53-c2af-e063-6294a90a6188 spl set id: 86ff4875-9007-4b7b-8f46-16cbd475d4bb

Reported adverse events (FAERS/openFDA)#

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