REVIVE 1
- Product NDC
- 69678-232
- 11-digit product format
- 696780232
- Labeler code
- 69678
- Product ID
- 69678-232_68339a6b-5993-4fd6-ad33-56de341762df
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- EEZAWAY RELIEF INC
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-10-01
- Marketing end
- 0000-00-00
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 3 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 69678-232-03 | REVIVE 1 | 88.7 mL in 1 BOTTLE | LIQUID | 88.7 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69678-232 | REVIVE 1 (MENTHOL) LIQUID [EEZAWAY RELIEF INC] | 1 | Legacy NDC, 1 package rows | 20211102_3efe50b9-737f-449b-a5d9-4fcf1bbd89c3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69678-232-03 | 69678023203 | 88.7 mL in 1 BOTTLE (69678-232-03) | 88.7 ml | 2021-10-01 | 0000-00-00 | No | No | Current |