Ice Gel
- Product NDC
- 52000-220
- 11-digit product format
- 520000220
- Labeler code
- 52000
- Product ID
- 52000-220_4f921d12-fa0b-7856-e063-6394a90ad55c
- 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
- 2018-04-02
- Substance
- MENTHOL
- Active strength
- 1.25 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ice Gel
- Brand name suffix
- ICE COLD ANALGESIC
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 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 |
|---|
| 52000-220-01 | Ice GelICE COLD ANALGESIC | 227 g in 1 JAR | GEL | 227 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 52000-220-01 | 52000022001 | 227 g in 1 JAR (52000-220-01) | 227 g | 2018-04-02 | No | No | Historical |