Thritex
- Product NDC
- 69440-008
- 11-digit product format
- 694400008
- Labeler code
- 69440
- Product ID
- 69440-008_ff4b111d-47cb-490d-8122-af553944dc5d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol
- Dosage form
- PATCH
- Route
- TOPICAL
- Labeler
- Binger Consulting Corporation
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2015-01-01
- Marketing end
- 0000-00-00
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 5 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69440-008-15 | Thritex | 15 in 1 BOX | PATCH | 15 | | 5 |
| 69440-008-15 | Thritex | 100 g in 1 PATCH | PATCH | 100 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69440-008 | THRITEX (MENTHOL) PATCH [BINGER CONSULTING CORPORATION] | 5 | Legacy NDC, 2 package rows | 20241129_32aca040-37f7-4195-8a5f-332d589a64d8.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 |
|---|
| 69440-008-15 | 69440000815 | 15 PATCH in 1 BOX (69440-008-15) > 100 g in 1 PATCH | 15 patch | 2015-01-01 | 0000-00-00 | No | No | Current |