NDC 0363-9890

SEVERE SINUS CONGESTION AND COUGH DAYTIME NON-DROWSY / NIGHTIME

Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride / Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, Phenylephrine Hydrochloride

SEVERE SINUS CONGESTION AND COUGH DAYTIME NON-DROWSY / NIGHTIME is a Kit in the Human Otc Drug category. It is labeled and distributed by Walgreens. The primary component is .

• Product ID: 0363-9890_60276fcc-ae8d-7ead-e053-2991aa0a5ada
• NDC: 0363-9890
• Product Type: Human Otc Drug
• Proprietary Name: SEVERE SINUS CONGESTION AND COUGH DAYTIME NON-DROWSY / NIGHTIME
• Generic Name: Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride / Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, Phenylephrine Hydrochloride
• Dosage Form: Kit
• Marketing Start Date: 2015-08-15
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Labeler Name: Walgreens
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0363-9890-20

1 KIT in 1 CARTON (0363-9890-20) * 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

• Marketing Start Date: 2017-12-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0363-9890-20 [00363989020]

SEVERE SINUS CONGESTION AND COUGH DAYTIME NON-DROWSY / NIGHTIME KIT

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2017-12-15

Drug Details

OpenFDA Data

• SPL SET ID: a016cf1c-a1b7-46a4-bda0-a5875e1be357
• Manufacturer:
  • Walgreens
• RxNorm Concept Unique ID - RxCUI:
  • 1086997
  • 1297404
  • 1297288