Robitussin Direct Sore Throat Pain
- Product NDC
- 0031-9301
- 11-digit product format
- 000319301
- Labeler code
- 0031
- Product ID
- 0031-9301_159c0477-cdc8-fbc7-e063-6294a90a3448
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Haleon US Holdings LLC
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-07-15
- Substance
- ACETAMINOPHEN
- Active strength
- 500 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Robitussin Direct Sore Throat Pain
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 198440 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0031-9301-01 | Robitussin Direct Sore Throat Pain | 18 in 1 BOTTLE | TABLET, COATED | 18 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0031-9301 | ROBITUSSIN DIRECT SORE THROAT PAIN (ACETAMINOPHEN) TABLET, COATED [HALEON US HOLDINGS LLC] | 4 | Current NDC, Legacy NDC, 1 package rows | 20240410_1b512078-24c3-4b80-8f2c-d6824d367f25.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0031-9301-01 | 00031930101 | 18 TABLET, COATED in 1 BOTTLE (0031-9301-01) | 2022-07-15 | 0000-00-00 | No | No | Current |