ANTIGRIP Daytime

Generic: Acetaminophen, Dextromethorphan HBr , Phenylephrine HCI

Labeler: Pharmadel LLC
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive

Drug Facts

Product Profile

Brand Name ANTIGRIP Daytime
Generic Name Acetaminophen, Dextromethorphan HBr , Phenylephrine HCI
Labeler Pharmadel LLC
Dosage Form POWDER, FOR SOLUTION
Routes
ORAL
Active Ingredients

ACETAMINOPHEN 650 mg/1, DEXTROMETHORPHAN HYDROBROMIDE 20 mg/1, PHENYLEPHRINE HYDROCHLORIDE 10 mg/1

Identifiers & Regulatory

Product NDC 55758-314
Product ID 55758-314_4549b549-8b9a-5fe8-e063-6394a90aca14
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Marketing Start 2019-03-28
Marketing End 2026-03-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55758314
Hyphenated Format 55758-314

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 ANTIGRIP Daytime (source: ndc)
Generic Name Acetaminophen, Dextromethorphan HBr , Phenylephrine HCI (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
  • 20 mg/1
  • 10 mg/1
source: ndc
Packaging
  • 18 POUCH in 1 CARTON (55758-314-18) / 1 POWDER, FOR SOLUTION in 1 POUCH
source: ndc

Packages (1)

Ingredients (3)

ACETAMINOPHEN (650 mg/1) DEXTROMETHORPHAN HYDROBROMIDE (20 mg/1) PHENYLEPHRINE HYDROCHLORIDE (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4549b549-8b9a-5fe8-e063-6394a90aca14", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1659967"], "spl_set_id": ["853012b8-d3b7-78d3-e053-2a91aa0ab0f2"], "manufacturer_name": ["Pharmadel LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "18 POUCH in 1 CARTON (55758-314-18)  / 1 POWDER, FOR SOLUTION in 1 POUCH", "package_ndc": "55758-314-18", "marketing_end_date": "20260301", "marketing_start_date": "20190328"}], "brand_name": "ANTIGRIP Daytime", "product_id": "55758-314_4549b549-8b9a-5fe8-e063-6394a90aca14", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "55758-314", "generic_name": "Acetaminophen, Dextromethorphan HBr , Phenylephrine HCI", "labeler_name": "Pharmadel LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ANTIGRIP Daytime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20260301", "marketing_start_date": "20190328"}