Childrens Tussin DM
- Product NDC
- 71027-032
- 11-digit product format
- 710270032
- Labeler code
- 71027
- Product ID
- 71027-032_79bd8e8f-7f05-4de4-8bbb-4b379df78957
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Childrens Tussin DM
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- KINGSTON PHARMA LLC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-03-01
- Marketing end
- 0000-00-00
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
- Active strength
- 5 mg/5mL; mg/5mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 71027-032-04 | Childrens Tussin DM | 118 mL in 1 BOTTLE | LIQUID | 118 | | 1 |
| 71027-032-04 | Childrens Tussin DM | 1 in 1 CARTON | LIQUID | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71027-032 | CHILDRENS TUSSIN DM LIQUID [KINGSTON PHARMA LLC] | 1 | Legacy NDC, 2 package rows | 20170319_79bd8e8f-7f05-4de4-8bbb-4b379df78957.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 71027-032-04 | 71027003204 | 118 mL in 1 BOTTLE | 118 ml | Historical |