999 ITCH RELIEF
- Product NDC
- 12753-930
- 11-digit product format
- 127530930
- Labeler code
- 12753
- Product ID
- 12753-930_1a9c76a3-1488-47f4-b75c-14e2bef779f3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- China Resources Sanjiu Medical & Pharmaceutical Co Ltd
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2003-07-03
- Marketing end
- 0000-00-00
- Substance
- MENTHOL; CAMPHOR (SYNTHETIC); DEXAMETHASONE
- Active strength
- 200 mg/20000mg; mg/20000mg; mg/20000mg
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 12753-930-19 | 999 ITCH RELIEF | 20000 mg in 1 CARTON | OINTMENT | 20000 | | 2991 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 12753-930 | 999 ITCH RELIEF (MENTHOL) OINTMENT [CHINA RESOURCES SANJIU MEDICAL & PHARMACEUTICAL CO LTD] | 2991 | Legacy NDC, 1 package rows | 20131022_d2390d79-4a64-4773-926b-3ebcdc0727f9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 12753-930-19 | 12753093019 | 20000 mg in 1 CARTON | 20000 mg | Historical |