Universal Ice Cold Analgesic
- Product NDC
- 52000-106
- 11-digit product format
- 520000106
- Labeler code
- 52000
- Product ID
- 52000-106_b89ff727-4759-4299-ae51-29faad8a69dd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Universal Distribution Center LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-05-01
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 1.25 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Universal Ice Cold Analgesic
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL, UNSPECIFIED FORM | 1.25 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 866128 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 52000-106-01 | Universal Ice Cold Analgesic | 237 mL in 1 TUBE | GEL | 237 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52000-106 | UNIVERSAL ICE COLD ANALGESIC (MENTHOL) GEL [UNIVERSAL DISTRIBUTION CENTER LLC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231122_79ad55eb-b59d-4bb8-88e3-3b51e10a7f28.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 |
|---|
| 52000-106-01 | 52000010601 | 237 mL in 1 TUBE (52000-106-01) | 237 ml | 2020-05-01 | 0000-00-00 | No | No | Current |