DayQuil Severe
- Product NDC
- 73097-006
- 11-digit product format
- 730970006
- Labeler code
- 73097
- Product ID
- 73097-006_8d6e93c1-81d3-d168-e053-2995a90a38c7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Savings Distributors LLC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2019-07-05
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 325 mg/1; mg/1; mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73097-006 | DAYQUIL SEVERE (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE) TABLET [SAVINGS DISTRIBUTORS LLC] | 1 | Legacy NDC, 6 package rows | 20190712_8d6e81d0-34ad-7617-e053-2a95a90a7695.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 73097-006-02 | 73097000602 | 1 in 1 CARTON | Historical |
| 73097-006-40 | 73097000640 | 20 in 1 CARTON | Historical |
| 73097-006-50 | 73097000650 | 2 in 1 POUCH | Historical |