Povidone-Iodine Prep Pad
- Product NDC
- 72059-002
- 11-digit product format
- 720590002
- Labeler code
- 72059
- Product ID
- 72059-002_6428a664-9e20-83c5-e053-2991aa0a4098
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Povidone-Iodine
- Dosage form
- SWAB
- Route
- PERCUTANEOUS
- Labeler
- Nantong Sirius Packing Products Co., Ltd.
- Application
- part333C
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-02-01
- Marketing end
- 0000-00-00
- Substance
- POVIDONE-IODINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72059-002-01 | Povidone-Iodine Prep Pad | 1 in 1 PACKAGE | SWAB | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72059-002 | POVIDONE-IODINE PREP PAD (POVIDONE-IODINE) SWAB [NANTONG SIRIUS PACKING PRODUCTS CO., LTD.] | 1 | Legacy NDC, 1 package rows | 20180201_64289d57-530b-60e3-e053-2a91aa0aa17c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 72059-002-01 | 72059000201 | 1 in 1 PACKAGE | Historical |