CALAMINE- ferric oxide red lotion

Calamine by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredients

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

SPL UNCLASSIFIED SECTION

Manufactured by Vi-Jon, Inc.

St. Louis, MO 63114

Questions or Comments?  1-888-593-0593

Made in the USA with US and foreign parts

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NDC: 0869-0063-30

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Calamine

Lotion

• Calamine Topical Suspension USP
• Skin Protectant
• Poison Ivy, Oak, Sumac Drying Lotion

6 FL OZ (177 mL)

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Mountain Falls 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: 0869-0063
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	80 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	80 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: 0869-0063-30	177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/15/1998
2	NDC: 0869-0063-26	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/15/1998
3	NDC: 0869-0063-34	237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/15/1998

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	07/15/1989

Labeler - Vi Jon (790752542)

Registrant - Vi Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi Jon		790752542	manufacture(0869-0063)