Tussin Cough and Chest Congestion DM
- Product NDC
- 11822-1173
- 11-digit product format
- 118221173
- Labeler code
- 11822
- Product ID
- 11822-1173_16c3f8f8-2bb7-482c-9aa1-0dc4ea2b80f0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dextromethorphan HBr, Guaifenesin
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-11-19
- Marketing end
- 0000-00-00
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
- Active strength
- 20 mg/10mL; mg/10mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-1173 | TUSSIN COUGH AND CHEST CONGESTION DM ADULT (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [RITE AID CORPORATION] | 3 | Legacy NDC | 20241113_b3fc7747-9994-4848-8d2a-721a489efffb.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-1173-7 | 11822117307 | 1 BOTTLE, PLASTIC in 1 BOX (11822-1173-7) > 118 mL in 1 BOTTLE, PLASTIC | 2021-11-19 | 0000-00-00 | No | No | Current |