Thiosinaminum
- Product NDC
- 71919-819
- 11-digit product format
- 719190819
- Labeler code
- 71919
- Product ID
- 71919-819_2cc890bb-e861-a6b1-e063-6394a90a494d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALLYLTHIOUREA
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Washington Homeopathic Products
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2023-11-08
- Substance
- ALLYLTHIOUREA
- Active strength
- 30 [hp_C]/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Thiosinaminum
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALLYLTHIOUREA | 30 [hp_C]/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 706IDJ14B7 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71919-819-01 | Thiosinaminum | 350 in 1 VIAL, GLASS | PELLET | 350 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71919-819 | THIOSINAMINUM (ALLYLTHIOUREA) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS] | 2 | Current NDC, 1 package rows | 20250130_09a60d62-a479-0f02-e063-6294a90a6d39.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71919-819-01 | 71919081901 | 350 PELLET in 1 VIAL, GLASS (71919-819-01) | 350 pellet | 2023-11-08 | No | No | Historical |