Blue Ice Topical Analgesic Gel
- Product NDC
- 52862-901
- 11-digit product format
- 528620901
- Labeler code
- 52862
- Product ID
- 52862-901_397ce4f6-f5af-18f1-e063-6394a90ad7c5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ice Gel
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- International Wholesale
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-01-01
- Substance
- CAMPHOR (SYNTHETIC); MENTHOL
- Active strength
- .5; 1 g/100g; 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
- Blue Ice Topical Analgesic Gel
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CAMPHOR (SYNTHETIC) | .5 g/100g |
| MENTHOL | 1 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5TJD82A1ET, L7T10EIP3A |
| Rxcui | 1043046 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 52862-901-01 | Blue Ice Topical Analgesic Gel | 227 g in 1 TUBE | 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 |
|---|
| 52862-901-01 | 52862090101 | 227 g in 1 TUBE (52862-901-01) | 227 g | 2024-01-01 | No | No | Current |