NDC | 63868-230-08 |
Set ID | 9fa49a3c-ad09-4d35-8cd9-e1a0f2da0d2d |
Category | HUMAN OTC DRUG LABEL |
Packager | Chain Drug Market Association |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333A |
- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Use
- Warnings
- Ask a doctor before use if you have
- Stop use and consult a doctor if
- When using this product do not
- Keep out of reach of children.
- Directions
- Inactive Ingredients
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
QUALITY CHOICE POVIDONE IODINE
povidone iodine 10% liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-230 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE 100 mg in 1 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) GLYCERIN (UNII: PDC6A3C0OX) NONOXYNOL-9 (UNII: 48Q180SH9T) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63868-230-08 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/12/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/01/2008 Labeler - Chain Drug Market Association (011920774) Registrant - Humco Holding Group, Inc. (825672884) Establishment Name Address ID/FEI Business Operations Humco Holding Group, Inc. 825672884 manufacture(63868-230) , analysis(63868-230) , pack(63868-230) , label(63868-230)