NUMOTIZINE
- Product NDC
- 10546-100
- 11-digit product format
- 105460100
- Labeler code
- 10546
- Product ID
- 10546-100_082b1721-9122-222f-e063-6294a90a5ea7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Hobart Laboratories, Inc.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2011-11-30
- Substance
- MENTHOL
- Active strength
- 1.25 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- NUMOTIZINE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 1.25 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 1233196, 1233201 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10546-100-08 | NUMOTIZINE | 228 g in 1 JAR | OINTMENT | 228 | | 8 |
| 10546-100-35 | NUMOTIZINE | 99 g in 1 JAR | OINTMENT | 99 | | 8 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10546-100 | NUMOTIZINE (MENTHOL) OINTMENT [HOBART LABORATORIES, INC.] | 8 | Current NDC, Legacy NDC, 2 package rows | 20231021_9a29ad1b-4ba3-403f-90c9-ee7582fe4535.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 |
|---|
| 10546-100-08 | 10546010008 | 228 g in 1 JAR (10546-100-08) | 228 g | 2011-11-30 | 0000-00-00 | No | No | Current |
| 10546-100-35 | 10546010035 | 99 g in 1 JAR (10546-100-35) | 99 g | 2011-11-30 | 0000-00-00 | No | No | Current |