sinus congestion and pain daytime non-drowsy

Generic: acetaminophen, phenylephrine hydrochloride

Labeler: h e b
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name sinus congestion and pain daytime non-drowsy
Generic Name acetaminophen, phenylephrine hydrochloride
Labeler h e b
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1, phenylephrine hydrochloride 5 mg/1

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-466
Product ID 37808-466_787f9336-f561-438a-9702-d74372b1eee7
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2005-07-26

Pharmacologic Class

Classes
adrenergic alpha1-agonists [moa] alpha-1 adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808466
Hyphenated Format 37808-466

Supplemental Identifiers

RxCUI
1046378
UPC
0041220360062
UNII
362O9ITL9D 04JA59TNSJ

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name sinus congestion and pain daytime non-drowsy (source: ndc)
Generic Name acetaminophen, phenylephrine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 5 mg/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 CARTON (37808-466-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

37808-466-08 2 BLISTER PACK in 1 CARTON (37808-466-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (2)

acetaminophen (325 mg/1) phenylephrine hydrochloride (5 mg/1)

Linked Drug Pages (1)

Sinus Congestion and Pain Daytime Non-Drowsy ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "787f9336-f561-438a-9702-d74372b1eee7", "openfda": {"upc": ["0041220360062"], "unii": ["362O9ITL9D", "04JA59TNSJ"], "rxcui": ["1046378"], "spl_set_id": ["e9dd2d7b-0a19-4a42-b51e-b9914f02406e"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (37808-466-08)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "37808-466-08", "marketing_start_date": "20050726"}], "brand_name": "Sinus Congestion and Pain Daytime Non-Drowsy", "product_id": "37808-466_787f9336-f561-438a-9702-d74372b1eee7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "37808-466", "generic_name": "Acetaminophen, Phenylephrine Hydrochloride", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sinus Congestion and Pain", "brand_name_suffix": "Daytime Non-Drowsy", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20050726", "listing_expiration_date": "20261231"}