Benzoin Tincture
- Product NDC
- 0395-0247
- 11-digit product format
- 003950247
- Labeler code
- 0395
- Product ID
- 0395-0247_0c929258-b192-bc2f-e063-6394a90a8e47
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzoin Resin
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Humco Holding Group, Inc.
- 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
- 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 |
|---|
| 0395-0247-92 | Benzoin Tincture | 59 mL in 1 BOTTLE, PLASTIC | LIQUID | 59 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0395-0247 | BENZOIN TINCTURE (BENZOIN RESIN) LIQUID [HUMCO HOLDING GROUP, INC.] | 5 | Current NDC, Legacy NDC, 1 package rows | 20231216_b33b5896-673b-498c-8a58-76ece8552f7a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0395-0247-92 | 00395024792 | 59 mL in 1 BOTTLE, PLASTIC (0395-0247-92) | 59 ml | 2017-11-10 | 0000-00-00 | No | No | Current |