Multi Symptom NightTime Cold
- Product NDC
- 69842-506
- 11-digit product format
- 698420506
- Labeler code
- 69842
- Product ID
- 69842-506_9f35dd1a-cc20-4aed-824f-8604692d4643
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen Diphenhydramine HCI Phenylephrine HCI
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- CVS Pharmacy
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-04-30
- Marketing end
- 2025-04-30
- Substance
- ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 325 mg/10mL; mg/10mL; mg/10mL
- Pharmacologic classes
- Adrenergic alpha1-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-1 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69842-506-04 | 69842050604 | 1 BOTTLE, PLASTIC in 1 BOX (69842-506-04) > 118 mL in 1 BOTTLE, PLASTIC | 2018-04-30 | 2025-04-30 | No | No | Current |