Analgesic
- Product NDC
- 61010-8201
- 11-digit product format
- 610108201
- Labeler code
- 61010
- Product ID
- 61010-8201_10981167-c8a2-e068-e063-6394a90ab165
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- menthol
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Safetec of America, Inc.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-09-01
- Substance
- MENTHOL
- Active strength
- 70 mg/L
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Analgesic
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 70 mg/L |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61010-8201-0 | Analgesic | 0.059 L in 1 BOTTLE, SPRAY | SPRAY | 0.059 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61010-8201 | ANALGESIC (MENTHOL) SPRAY [SAFETEC OF AMERICA, INC.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20240214_79e3b0e7-4ba5-4b9d-a980-5b6f18dba802.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61010-8201-0 | 61010820100 | .059 L in 1 BOTTLE, SPRAY (61010-8201-0) | 2018-09-01 | 0000-00-00 | No | No | Current |