Betadine
- Product NDC
- 67618-192
- 11-digit product format
- 676180192
- Labeler code
- 67618
- Product ID
- 67618-192_b8f5797b-73e1-4201-b824-2cdd50c90497
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- POVIDONE-IODINE
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Atlantis Consumer Healthcare, Inc.
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-01-02
- Substance
- POVIDONE-IODINE
- Active strength
- 5 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Betadine
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POVIDONE-IODINE | 5 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 85H0HZU99M |
| Rxcui | 108204, 238850 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67618-192-03 | Betadine | 88.7 mL in 1 BOTTLE | SPRAY | 88.7 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67618-192 | BETADINE (POVIDONE-IODINE) SPRAY [ATLANTIS CONSUMER HEALTHCARE, INC.] | 1 | Current NDC, 1 package rows | 20250104_00002127-02bc-4c66-b0c3-ca29d8224afc.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 67618-192-03 | 67618019203 | 88.7 mL in 1 BOTTLE (67618-192-03) | 88.7 ml | 2025-01-02 | No | No | Current |