Benzoin Tincture
- Product NDC
- 82645-924
- 11-digit product format
- 826450924
- Labeler code
- 82645
- Product ID
- 82645-924_0d6cc91d-1d9b-25ae-e063-6394a90aa6a0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzoin Resin
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Pharma Nobis, 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
- 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 |
|---|
| 82645-924-92 | Benzoin Tincture | 59 mL in 1 BOTTLE, PLASTIC | LIQUID | 59 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82645-924 | BENZOIN TINCTURE (BENZOIN RESIN) LIQUID [PHARMA NOBIS, LLC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231227_e42fccc2-1b4f-e7f3-e053-2a95a90aef39.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 82645-924-92 | 82645092492 | 59 mL in 1 BOTTLE, PLASTIC (82645-924-92) | 59 ml | 2017-12-12 | 0000-00-00 | No | No | Current |