Benzoin Compound Tincture
- Product NDC
- 54162-100
- 11-digit product format
- 541620100
- Labeler code
- 54162
- Product ID
- 54162-100_e89b0485-f044-4ed2-bf0f-ad85460d8bc2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZOIN RESIN
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Geritrex LLC
- Application
- part356
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2015-07-31
- Marketing end
- 0000-00-00
- Substance
- BENZOIN RESIN
- Active strength
- 100 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 54162-100-01 | Benzoin Compound Tincture | 29 mL in 1 BOTTLE, PLASTIC | LIQUID | 29 | | 4 |
| 54162-100-02 | Benzoin Compound Tincture | 58 mL in 1 BOTTLE, PLASTIC | LIQUID | 58 | | 4 |
| 54162-100-04 | Benzoin Compound Tincture | 118 mL in 1 BOTTLE, PLASTIC | LIQUID | 118 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 54162-100 | BENZOIN COMPOUND TINCTURE (BENZOIN RESIN) LIQUID [GERITREX LLC] | 4 | Legacy NDC, 3 package rows | 20180119_52ac98db-f466-4419-ac03-5624b7503083.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 54162-100-01 | 54162010001 | 29 mL in 1 BOTTLE, PLASTIC | 29 ml | Historical |
| 54162-100-02 | 54162010002 | 58 mL in 1 BOTTLE, PLASTIC | 58 ml | Historical |
| 54162-100-04 | 54162010004 | 118 mL in 1 BOTTLE, PLASTIC | 118 ml | Historical |