Cold Spot
- Product NDC
- 65121-002
- 11-digit product format
- 651210002
- Labeler code
- 65121
- Product ID
- 65121-002_d07db448-ed4d-4c49-bc25-23400c5d95bc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- menthol
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Pure Source
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2010-08-24
- Marketing end
- 0000-00-00
- Substance
- MENTHOL
- Active strength
- 13 mL/90mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 65121-002-03 | Cold SpotPoint Relief | 90 mL in 1 BOTTLE | OINTMENT | 90 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 65121-002 | COLD SPOT POINT RELIEF (MENTHOL) OINTMENT [PURE SOURCE] | 2 | Legacy NDC, 1 package rows | 20101013_fde00a95-7bc2-4da6-8d08-d7d673313a3c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 65121-002-03 | 65121000203 | 90 mL in 1 BOTTLE | 90 ml | Historical |