Adult Cough Relief DM
- Product NDC
- 21130-383
- 11-digit product format
- 211300383
- Labeler code
- 21130
- Product ID
- 21130-383_155100dc-a514-4896-94f9-a3bbd8fb20ce
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dextromethorphan HBr
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Safeway, Inc.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2014-06-30
- Marketing end
- 2025-06-30
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE
- Active strength
- 30 mg/10mL
- Pharmacologic classes
- Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| DEXTROMETHORPHAN HYDROBROMIDE | ACTIVE INGREDIENT | 9D2RTI9KYH | ADULT COUGH RELIEF DM (DEXTROMETHORPHAN HBR) LIQUID [SAFEWAY, INC.] | 3 | |
| DEXTROMETHORPHAN | ACTIVE MOIETY | 7355X3ROTS | ADULT COUGH RELIEF DM (DEXTROMETHORPHAN HBR) LIQUID [SAFEWAY, INC.] | 3 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | ADULT COUGH RELIEF DM (DEXTROMETHORPHAN HBR) LIQUID [SAFEWAY, INC.] | 3 | |
| ANHYDROUS CITRIC ACID | INACTIVE INGREDIENT | XF417D3PSL | ADULT COUGH RELIEF DM (DEXTROMETHORPHAN HBR) LIQUID [SAFEWAY, INC.] | 3 | |
| FD&C RED NO. 40 | INACTIVE INGREDIENT | WZB9127XOA | ADULT COUGH RELIEF DM (DEXTROMETHORPHAN HBR) LIQUID [SAFEWAY, INC.] | 3 | |
| GLUCOSE OXIDASE | INACTIVE INGREDIENT | 0T8392U5N1 | ADULT COUGH RELIEF DM (DEXTROMETHORPHAN HBR) LIQUID [SAFEWAY, INC.] | 3 | |
| GLYCERIN | INACTIVE INGREDIENT | PDC6A3C0OX | ADULT COUGH RELIEF DM (DEXTROMETHORPHAN HBR) LIQUID [SAFEWAY, INC.] | 3 | |
| HIGH FRUCTOSE CORN SYRUP | INACTIVE INGREDIENT | XY6UN3QB6S | ADULT COUGH RELIEF DM (DEXTROMETHORPHAN HBR) LIQUID [SAFEWAY, INC.] | 3 | |
| MENTHOL, UNSPECIFIED FORM | INACTIVE INGREDIENT | L7T10EIP3A | ADULT COUGH RELIEF DM (DEXTROMETHORPHAN HBR) LIQUID [SAFEWAY, INC.] | 3 | |
| SACCHARIN SODIUM | INACTIVE INGREDIENT | SB8ZUX40TY | ADULT COUGH RELIEF DM (DEXTROMETHORPHAN HBR) LIQUID [SAFEWAY, INC.] | 3 | |
| SODIUM BENZOATE | INACTIVE INGREDIENT | OJ245FE5EU | ADULT COUGH RELIEF DM (DEXTROMETHORPHAN HBR) LIQUID [SAFEWAY, INC.] | 3 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | ADULT COUGH RELIEF DM (DEXTROMETHORPHAN HBR) LIQUID [SAFEWAY, INC.] | 3 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21130-383 | ADULT COUGH RELIEF DM (DEXTROMETHORPHAN HBR) LIQUID [SAFEWAY, INC.] | 7 | Legacy NDC | 20221110_312749dc-8e60-4cab-9054-e8f04a5e9dfc.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 21130-383-04 | 21130038304 | 1 BOTTLE, PLASTIC in 1 BOX (21130-383-04) > 118 mL in 1 BOTTLE, PLASTIC | 2014-06-30 | 2025-06-30 | No | No | Current |