UtaSpray
- Product NDC
- 82198-0008
- 11-digit product format
- 821980008
- Labeler code
- 82198
- Product ID
- 82198-0008_0aa37a7b-851a-d9d5-e063-6294a90a23be
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol and Methyl Salicylate
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Big 5 Nutrition LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-10-01
- Substance
- MENTHOL; METHYL SALICYLATE
- Active strength
- 100; 50 mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- UtaSpray
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 100 mg/mL |
| METHYL SALICYLATE | 50 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A, LAV5U5022Y |
| Rxcui | 1875611 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82198-0008-1 | UtaSpray | 70 mL in 1 BOTTLE | LIQUID | 70 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82198-0008 | UTASPRAY (MENTHOL AND METHYL SALICYLATE) LIQUID [BIG 5 NUTRITION LLC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231122_c641ab11-cd00-4e23-ace7-8178739084f0.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 |
|---|
| 82198-0008-1 | 82198000801 | 70 mL in 1 BOTTLE (82198-0008-1) | 70 ml | 2022-10-01 | 0000-00-00 | No | No | Current |