Label: IODINE TINCTURE WHITE- iodine tincture solution/ drops
- NDC Code(s): 70242-109-01
- Packager: Dannso Corp./d.b.a. Essential Products
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 1, 2023
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Use
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WARNINGS
Warnings
For external use only. Avoid contact with eyes or with mucous membrane. Keep out of the reach of children. Children under 2 years please consult a physician. Do not apply on irritated skin, in or near eyes or mocuos memebranes, on wounds or damamged skin, or if it causes allergic reaction. In case of accidental ingestion, seek professional assistance or contact Poison Control Center immedialately.
- Inactive Ingredient
- Stop use and ask a doctor
- Keep out of reach of children
- Directions
- Questions or Comments?
- Principal display panel
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INGREDIENTS AND APPEARANCE
IODINE TINCTURE WHITE
iodine tincture solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70242-109 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength AMMONIUM SALICYLATE (UNII: 0T3Q181657) Isopropyl Alcohol (UNII: ND2M416302) Sodium Iodide (UNII: F5WR8N145C) water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70242-109-01 30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/08/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 08/08/2015 Labeler - Dannso Corp./d.b.a. Essential Products (059741071) Registrant - Dannso Corp./d.b.a. Essential Products (059741071) Establishment Name Address ID/FEI Business Operations World Perfume, Inc 101312044 MANUFACTURE(70242-109)