CALAMINE- ferric oxide red lotion

Calamine by

Drug Labeling and Warnings

Calamine by is a Otc medication manufactured, distributed, or labeled by Walgreen Co., Vi Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredents

Calamine 8%
Zinc oxide 8%

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 a 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

• shake well before using
• apply as needed

Other information

store at 59⁰ - 86⁰ F

Inactive ingredients

bentonite magma, calcium hydroxide, glycerin, purified water

Questions

1-888-593-0593

Disclaimer

Walgreens Pharmacist Recommended

Walgreens Pharmacist Survey Study, November 2016

adverse reactions

DISTRIBUTED BY: WALGREEN CO.

200 WILMOT RD., DEERFIELD, IL

100% SATISFACTION GUARANTEED

walgreens.com  2016 Walgreen Co

MADE IN U.S.A. WITH U.S. AND FOREIGN COMPENENTS

Principal Display Panel

Walgreens

Calamine

Lotion

CALAMINE TOPICAL

SUSPENSION USP/

SKIN PROTECTANT

• Poison ivy, oak & sumac drying lotion

6 FL OZ (177 mL)

INGREDIENTS AND APPEARANCE

CALAMINE  
ferric oxide red lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-0224
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FERRIC OXIDE RED (UNII: 1K09F3G675) (FERRIC OXIDE RED - UNII:1K09F3G675)	FERRIC OXIDE RED	8 g  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	8 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BENTONITE (UNII: A3N5ZCN45C)
CALCIUM HYDROXIDE (UNII: PF5DZW74VN)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-0224-30	177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/05/1996

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	01/05/1996

Labeler - Walgreen Co. (008965063)

Registrant - Vi Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi Jon		790752542	manufacture(0363-0224)