Package 0067-6095-03

Brand: theraflu powerpods nighttime severe cold

Generic: acetaminophen, diphenhydramine hcl, phenylephrine hcl
NDC Package

Package Facts

Identity

Package NDC 0067-6095-03
Digits Only 0067609503
Product NDC 0067-6095
Product ID 0067-6095_102bd52f-def1-ca60-e063-6294a90a1d4d
Description

1 POUCH in 1 CARTON (0067-6095-03) / 1 POWDER, FOR SOLUTION in 1 POUCH

Marketing

Marketing Status
Marketed Since 2019-01-20
Brand theraflu powerpods nighttime severe cold
Generic acetaminophen, diphenhydramine hcl, phenylephrine hcl
Sample Package No

Linked Drug Pages (1)

THERAFLU POWERPODS NIGHTTIME SEVERE COLD ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "102bd52f-def1-ca60-e063-6294a90a1d4d", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40", "04JA59TNSJ"], "rxcui": ["1659960"], "spl_set_id": ["39f9feef-4bf2-4f10-9fff-22bbb1d8a471"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "8 POUCH in 1 CARTON (0067-6095-01)  / 1 POWDER, FOR SOLUTION in 1 POUCH (0067-6095-02)", "package_ndc": "0067-6095-01", "marketing_start_date": "20180728"}, {"sample": false, "description": "1 POUCH in 1 CARTON (0067-6095-03)  / 1 POWDER, FOR SOLUTION in 1 POUCH", "package_ndc": "0067-6095-03", "marketing_start_date": "20190120"}], "brand_name": "THERAFLU POWERPODS NIGHTTIME SEVERE COLD", "product_id": "0067-6095_102bd52f-def1-ca60-e063-6294a90a1d4d", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "0067-6095", "generic_name": "ACETAMINOPHEN, DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCL", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "THERAFLU", "brand_name_suffix": "POWERPODS NIGHTTIME SEVERE COLD", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180728", "listing_expiration_date": "20261231"}