Label: DECOLORIZED IODINE- ethyl alcohol liquid
- NDC Code(s): 82645-909-91, 82645-909-92
- Packager: Pharma Nobis, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 22, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredients
- Purpose
- Uses
- Warnings
- Ask a doctor before use if you have
- Stop use and ask a doctor if:
- When using this product:
- Keep out of the reach of children.
- Directions
- Inactive Ingredient:
- Other Information:
- De La Cruz Label
- Good Neighbor Label
- Leader Label
- Quality Choice Label
- Sunmark Label
- DDM Label
- Rite Aid Label
- CVS Label
- Top Care Label
- Vida Mia Label
- Health Mart Label
-
INGREDIENTS AND APPEARANCE
DECOLORIZED IODINE
ethyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82645-909 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.45 mL in 1 mL Inactive Ingredients Ingredient Name Strength AMMONIA (UNII: 5138Q19F1X) IODINE (UNII: 9679TC07X4) POTASSIUM IODIDE (UNII: 1C4QK22F9J) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82645-909-92 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/23/2022 2 NDC:82645-909-91 30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/23/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 06/23/2022 Labeler - Pharma Nobis, LLC (118564114) Registrant - Pharma Nobis, LLC (118564114) Establishment Name Address ID/FEI Business Operations Pharma Nobis, LLC 118564114 manufacture(82645-909) , analysis(82645-909) , pack(82645-909) , label(82645-909)