Broncomar
- Product NDC
- 70242-103
- 11-digit product format
- 702420103
- Labeler code
- 70242
- Product ID
- 70242-103_79da1c58-44ee-43f6-a452-7b9047e5d278
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dextromethorphan HBr, Guaifenesin
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Dannso Corp./d.b.a. Essential Products
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2001-10-01
- Marketing end
- 0000-00-00
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
- Active strength
- 30 mg/10mL; mg/10mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70242-103-06 | BroncomarMaximun Cough Relief | 1 in 1 CARTON | LIQUID | 1 | | 4 |
| 70242-103-06 | BroncomarMaximun Cough Relief | 177 mL in 1 BOTTLE | LIQUID | 177 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70242-103 | BRONCOMAR MAXIMUN COUGH RELIEF (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [DANNSO CORP./D.B.A. ESSENTIAL PRODUCTS] | 4 | Legacy NDC, 2 package rows | 20200925_3a7986cd-b16e-4201-95b1-f53b9a6c2529.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70242-103-06 | 70242010306 | 1 BOTTLE in 1 CARTON (70242-103-06) > 177 mL in 1 BOTTLE | 1 bottle | 2015-01-01 | 0000-00-00 | No | No | Current |