BLITZ RELIEF
- Product NDC
- 72676-101
- 11-digit product format
- 726760101
- Labeler code
- 72676
- Product ID
- 72676-101_d607ac71-c00e-9d76-e053-2a95a90a210d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- CAMPHOR, MENTHOL
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- BLITZ PRODUCTS LLC
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-11-13
- Marketing end
- 0000-00-00
- Substance
- CAMPHOR (SYNTHETIC); MENTHOL
- Active strength
- 4 g/100mL; g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 72676-101-11 | BLITZ RELIEF | 29.57 mL in 1 BOTTLE, SPRAY | SPRAY | 29.57 | | 4 |
| 72676-101-12 | BLITZ RELIEF | 59 mL in 1 BOTTLE, SPRAY | SPRAY | 59 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72676-101 | BLITZ RELIEF (CAMPHOR, MENTHOL) SPRAY [BLITZ PRODUCTS LLC] | 4 | Legacy NDC, 2 package rows | 20220121_07db901c-8985-4700-b438-ac5fbb982947.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72676-101-11 | 72676010111 | 29.57 mL in 1 BOTTLE, SPRAY (72676-101-11) | 29.57 ml | 2020-11-13 | 0000-00-00 | No | No | Current |
| 72676-101-12 | 72676010112 | 59 mL in 1 BOTTLE, SPRAY (72676-101-12) | 59 ml | 2020-11-13 | 0000-00-00 | No | No | Current |