DUREX 7% TINCTURE IODINE LINIMENT [JACKS MFG INC]

DUREX 7% TINCTURE IODINE LINIMENT [JACKS MFG INC]
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NDC	61156-109-02
Set ID	50f3e73e-57ca-4d5b-923f-f2ce0cc7a057
Category	OTC ANIMAL DRUG LABEL
Packager	JACKS MFG INC
Generic Name
Product Class
Product Number
Application Number

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DIRECTIONS

For superficial cuts, bruises, abrasions, insect bites, etc.

Also for other external disinfection uses.

CAUTION

Avoid contact with eyes or mucous membranes.
Do not use on deep wounds or body cavities.
Do not use on burns.
WARNINGPOISON IF TAKEN INTERNALLY.

If accidentally ingested, call poison control immediately. Tighten cap firmly when not in use.

Do not use on animals intended for food.

Keep away from heat and open flame.

Wear hand and eye protection when handling.
Package Label

INGREDIENTS AND APPEARANCE

DUREX 7% TINCTURE IODINE
durex 7% tincture iodine liniment

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC:61156-109
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4)	IODINE	0.33 g in 1 mL

Ingredient Name	Strength
Inactive Ingredients
POTASSIUM IODIDE (UNII: 1C4QK22F9J)	0.22 g in 1 mL
ISOPROPYL ALCOHOL (UNII: ND2M416302)	3.67 mL in 1 mL
WATER (UNII: 059QF0KO0R)	0.94 mL in 1 mL
POVIDONE-IODINE (UNII: 85H0HZU99M)	0.03 g in 1 mL

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:61156-109-02	473 mL in 1 BOTTLE

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		07/01/1994

Labeler - JACKS MFG INC (056741838)

Registrant - JACKS MFG INC (056741838)

Name	Address	ID/FEI	Business Operations
Establishment
TENDA HORSE PRODUCTS, LLC		137337247	manufacture, api manufacture

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