Pressure plus Pain PE plus Mucus
- Product NDC
- 50804-006
- 11-digit product format
- 508040006
- Labeler code
- 50804
- Product ID
- 50804-006_e8b846bc-7203-21ef-e053-2995a90a2e55
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- GoodSense
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-05-30
- Marketing end
- 2024-12-31
- Substance
- ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 325 mg/1; mg/1; mg/1
- Pharmacologic classes
- Adrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], alpha-1 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50804-006-03 | 50804000603 | 2 BLISTER PACK in 1 CARTON (50804-006-03) > 12 TABLET, COATED in 1 BLISTER PACK | 2 blister pack | 2016-05-31 | 0000-00-00 | No | No | Current |