Label: BETADINE SOLUTION- povidone-iodine solution
-
NDC Code(s):
67618-150-01,
67618-150-04,
67618-150-05,
67618-150-09, view more67618-150-17, 67618-150-32
- Packager: Atlantis Consumer Healthcare, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 22, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctorif
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
BETADINE SOLUTION
povidone-iodine solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67618-150 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM HYDROXIDE (UNII: 55X04QC32I) C12-15 PARETH-9 (UNII: H3ZIY6WP1R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67618-150-09 237 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/01/1980 2 NDC:67618-150-05 14.8 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/01/1980 3 NDC:67618-150-04 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/01/1980 4 NDC:67618-150-17 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/01/1980 5 NDC:67618-150-32 946 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/01/1980 08/31/2024 6 NDC:67618-150-01 3780 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/01/1980 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 06/01/1980 Labeler - Atlantis Consumer Healthcare, Inc. (118983925) Registrant - Atlantis Consumer Healthcare, Inc. (118983925)