Simanix
- Product NDC
- 69379-001
- 11-digit product format
- 693790001
- Labeler code
- 69379
- Product ID
- 69379-001_1a4e1221-85ef-3579-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Simanix Pain Relieving Cream
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Home Aide Diagnostics, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2015-07-08
- Marketing end
- 0000-00-00
- Substance
- CAPSAICIN; MENTHOL; HISTAMINE DIHYDROCHLORIDE
- Active strength
- 0 g/100g; g/100g; g/100g
- 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 |
|---|
| 69379-001-03 | Simanix | 120 g in 1 BOTTLE | CREAM | 120 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69379-001 | SIMANIX (SIMANIX PAIN RELIEVING CREAM) CREAM [HOME AIDE DIAGNOSTICS, INC.] | 1 | Legacy NDC, 1 package rows | 20150708_1a4e1221-85ee-3579-e054-00144ff88e88.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 69379-001-03 | 69379000103 | 120 g in 1 BOTTLE | 120 g | Historical |