Country: United States
Language: English
Source: NLM (National Library of Medicine)
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4)
Publix
TOPICAL
OTC DRUG
Antiseptic First aid antiseptic to prevent infection in minor cuts and burns. - deep punture wounds - animal bites - serious burns - the condition persists or gets worse - irritation and redness develop and persits for more than 72 hours
OTC monograph not final
PUBLIX POVIDONE IODINE- POVIDONE IODINE 10% LIQUID PUBLIX ---------- PUBLIX POVIDONE IODINE Drug Facts ACTIVE INGREDIENT Povidone-Iodine 10% (Equivalent to 1% titrable iodine) PURPOSE Antiseptic USE First aid antiseptic to prevent infection in minor cuts and burns. WARNINGS For External Use Only ASK A DOCTOR BEFORE USE IF YOU HAVE deep punture wounds animal bites serious burns STOP USE AND CONSULT A DOCTOR IF the condition persists or gets worse irritation and redness develop and persits for more than 72 hours WHEN USING THIS PRODUCT DO NOT use in eyes use on individuals who are allergic or sensitive to iodine or use for longer thn 1 week unless directed by a doctor apply over large areas of the body KEEP OUT OF REACH OF CHILDREN. In case of accidental ingestion, seek professional assistance or 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 badaged, let it dry first. OTHER INFORMATION store at room temperature, 20-25C (68-77F) INACTIVE INGREDIENTS Citric Acid, Disodium Phosphate, Glycerin, nonoxynol-9. Sodium Hydroxide and Purified Water. LABEL PUBLIX POVIDONE IODINE povidone iodine 10% liquid PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:41415-325 ROUTE OF ADMINISTRATION TOPICAL Publix 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:41415- 325-98 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/30/2017 MARKETING INFORMATION MARKETING CATEGORY APPLICATION NUMBER OR MONOGRAPH CITATION MARKETING START DATE MARKETING END DATE OTC Monograph Drug M003 01 Read the complete document