NDC 67777-140

povidine iodine

Povidine Iodine

povidine iodine is a Topical Swab in the Human Otc Drug category. It is labeled and distributed by Dynarex Corporation. The primary component is Povidone-iodine.

• Product ID: 67777-140_56609c63-de60-4111-a317-4f0fc1db502b
• NDC: 67777-140
• Product Type: Human Otc Drug
• Proprietary Name: povidine iodine
• Generic Name: Povidine Iodine
• Dosage Form: Swab
• Route of Administration: TOPICAL
• Marketing Start Date: 2010-05-10
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part333
• Labeler Name: Dynarex Corporation
• Substance Name: POVIDONE-IODINE
• Active Ingredient Strength: 10 mL/100mL
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 67777-140-01

10 BOX in 1 CASE (67777-140-01) > 100 POUCH in 1 BOX > .3 mL in 1 POUCH

• Marketing Start Date: 2010-05-10
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 67777-140-01 [67777014001]

povidine iodine SWAB

• Marketing Category: OTC monograph final
• Application Number: part333
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2010-05-10
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
POVIDONE-IODINE	10 mL/100mL

OpenFDA Data

• SPL SET ID: e39ef99d-c778-4862-9d93-4074753c47ad
• Manufacturer:
  • Dynarex Corporation
• UNII:
  • 85H0HZU99M
• RxNorm Concept Unique ID - RxCUI:
  • 797730

NDC Crossover Matching brand name "povidine iodine" or generic name "Povidine Iodine"

NDC	Brand Name	Generic Name
0404-5637	povidine iodine	povidine iodine
0404-5638	povidine iodine	povidine iodine
0404-5639	povidine iodine	povidine iodine
67777-110	povidine iodine	povidine iodine
67777-130	povidine iodine	povidine iodine
67777-140	povidine iodine	povidine iodine
67777-301	povidine iodine	povidine iodine
67777-419	povidine iodine	povidine iodine
67777-420	povidine iodine	povidine iodine
68016-013	povidine iodine	povidine iodine
67777-100	povidone iodine	povidine iodine