Sunmark Benzoin Compound Tincture
- Product NDC
- 49348-138
- 11-digit product format
- 493480138
- Labeler code
- 49348
- Product ID
- 49348-138_0ce57521-f389-2c51-e063-6394a90a3b10
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzoin Resin
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2008-01-01
- 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
- Sunmark Benzoin Compound 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 Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 49348-138-30 | Sunmark Benzoin Compound Tincture | 59 mL in 1 BOTTLE, PLASTIC | LIQUID | 59 | | 7 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49348-138 | SUNMARK BENZOIN COMPOUND TINCTURE (BENZOIN RESIN) LIQUID [STRATEGIC SOURCING SERVICES LLC] | 7 | Current NDC, Legacy NDC, 1 package rows | 20231220_0c96d810-83dc-47d3-9a75-63a79feaad0a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49348-138-30 | 49348013830 | 59 mL in 1 BOTTLE, PLASTIC (49348-138-30) | 59 ml | 2017-12-12 | 0000-00-00 | No | No | Current |