Benzoin Tincture
- Product NDC
- 70677-1200
- 11-digit product format
- 706771200
- Labeler code
- 70677
- Product ID
- 70677-1200_29814e8e-aeff-1f54-e063-6294a90ab7f9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzoin Resin
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- 116956644
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-12-17
- Substance
- BENZOIN RESIN
- Active strength
- 1000 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
- Benzoin Tincture
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZOIN RESIN | 1000 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | GK21SBA74R |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70677-1200-1 | Benzoin Tincture | 59 mL in 1 BOTTLE, GLASS | LIQUID | 59 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70677-1200 | BENZOIN TINCTURE (BENZOIN RESIN) LIQUID [116956644] | 1 | Current NDC, 1 package rows | 20241220_2981217f-f250-c090-e063-6294a90a85b0.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70677-1200-1 | 70677120001 | 59 mL in 1 BOTTLE, GLASS (70677-1200-1) | 59 ml | 2024-12-17 | No | No | Current |