Quality Choice Iodine Tincture Mild (Iodine And Sodium Iodide And Alcohol) Liquid [Chain Drug Market Association] -

QUALITY CHOICE IODINE TINCTURE MILD (IODINE AND SODIUM IODIDE AND ALCOHOL) LIQUID [CHAIN DRUG MARKET ASSOCIATION]
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NDC	63868-330-01
Set ID	55c970ed-13a9-4ea2-a8cb-aaf14d3a214d
Category	HUMAN OTC DRUG LABEL
Packager	Chain Drug Market Association
Generic Name
Product Class
Product Number
Application Number	PART333A

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SPL UNCLASSIFIED SECTION

Drug Facts
Active ingredient

Iodine Tincture, USP 2%, Mild
Purpose

First Aid Antiseptic
Indications

First aid to help prevent infection in minor cuts, scrapes and burns
Warnings
For external use only.
Ask a doctor before use if you have
- deep or puncture wounds
- animal bites
- serious burns
- Flammable: Keep away from sparks heat and flame
Stop use and consult doctor if
- the condition persists or gets worse, or if using for longer than one week
When using this product
- do not use in the eyes. If contact occurs, flush with large amounts of water while lifting upper and lower lids
- do not apply over large areas of the body
Keep out of reach of children.

In case of accidental ingestion, give milk then a starch solution made by mixing two tablespoonfuls of cornstarch or flour to a pint of water. Contact a Poison Control Center immediately.
Directions
- clean the affected area
- apply a small amount on the area 1 to 3 times daily
- may be covered with sterile bandage
- if bandaged let dry first
Other information
- will stain skin and clothing
Inactive ingredient

none
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INGREDIENTS AND APPEARANCE

QUALITY CHOICE IODINE TINCTURE MILD
iodine and sodium iodide and alcohol liquid

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4)	IODINE	20 mg in 1 mL
SODIUM IODIDE (UNII: F5WR8N145C) (IODIDE ION - UNII:09G4I6V86Q)	IODIDE ION	20.4 mg in 1 mL
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	470 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:63868-330-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/12/2017

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	01/01/1979

Labeler - Chain Drug Market Association (011920774)

Registrant - Humco Holding Group, Inc. (825672884)

Name	Address	ID/FEI	Business Operations
Establishment
Humco Holding Group, Inc.		825672884	manufacture(63868-330) , analysis(63868-330) , pack(63868-330) , label(63868-330)

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