Universal Ice Cold Analgesic
- Product NDC
- 52000-105
- 11-digit product format
- 520000105
- Labeler code
- 52000
- Product ID
- 52000-105_58b2217d-5ab4-4db5-8b59-cac4a647b414
- 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
- 2020-01-25
- Substance
- MENTHOL, UNSPECIFIED FORM
- 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
- Universal Ice Cold Analgesic
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL, UNSPECIFIED FORM | 1.25 g/100g |
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 |
|---|
| 52000-105-01 | Universal Ice Cold Analgesic | 227 g in 1 BOTTLE, PLASTIC | GEL | 227 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52000-105 | UNIVERSAL ICE COLD ANALGESIC (MENTHOL) GEL [UNIVERSAL DISTRIBUTION CENTER LLC] | 3 | Current NDC, Legacy NDC, 1 package rows | 20231122_4fdf61d8-a9e0-4cd2-9e3f-0bdedc47a52f.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 |
|---|
| 52000-105-01 | 52000010501 | 227 g in 1 BOTTLE, PLASTIC (52000-105-01) | 227 g | 2020-01-25 | 0000-00-00 | No | No | Current |