daytime nighttime

Generic: acetaminophen, dextromethorphan hbr, phenylephrine hcl and acetaminophen, dextromethorphan hbr, doxylamine succinate

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

Drug Facts

Product Profile

Brand Name daytime nighttime
Generic Name acetaminophen, dextromethorphan hbr, phenylephrine hcl and acetaminophen, dextromethorphan hbr, doxylamine succinate
Labeler h-e-b
Dosage Form KIT
Routes
ORAL
Manufacturer
H-E-B

Identifiers & Regulatory

Product NDC 37808-191
Product ID 37808-191_f2335603-5091-11ca-e053-2995a90a7f34
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2022-06-20

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808191
Hyphenated Format 37808-191

Supplemental Identifiers

RxCUI
1086997 1094549 2634564

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 daytime nighttime (source: ndc)
Generic Name acetaminophen, dextromethorphan hbr, phenylephrine hcl and acetaminophen, dextromethorphan hbr, doxylamine succinate (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg
  • 10 mg
  • 5 mg
  • 15 mg
  • 6.25 mg
source: label
Packaging
  • 4 BLISTER PACK in 1 CARTON (37808-191-48) / 1 KIT in 1 BLISTER PACK * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
source: ndc

Packages (1)

37808-191-48 4 BLISTER PACK in 1 CARTON (37808-191-48) / 1 KIT in 1 BLISTER PACK * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Daytime Nighttime ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f2335603-5091-11ca-e053-2995a90a7f34", "openfda": {"rxcui": ["1086997", "1094549", "2634564"], "spl_set_id": ["db19b8c7-0334-0664-e053-2a95a90ad61f"], "manufacturer_name": ["H-E-B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (37808-191-48)  / 1 KIT in 1 BLISTER PACK *  8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK *  4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "37808-191-48", "marketing_start_date": "20220620"}], "brand_name": "Daytime Nighttime", "product_id": "37808-191_f2335603-5091-11ca-e053-2995a90a7f34", "dosage_form": "KIT", "product_ndc": "37808-191", "generic_name": "Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl and Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate", "labeler_name": "H-E-B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Daytime Nighttime", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220620", "listing_expiration_date": "20261231"}