theraflu powerpods nighttime severe cold
Generic: acetaminophen, diphenhydramine hcl, phenylephrine hcl
Labeler: haleon us holdings llcDrug Facts
Product Profile
Brand Name
theraflu powerpods nighttime severe cold
Generic Name
acetaminophen, diphenhydramine hcl, phenylephrine hcl
Labeler
haleon us holdings llc
Dosage Form
POWDER, FOR SOLUTION
Routes
Active Ingredients
acetaminophen 650 mg/1, diphenhydramine hydrochloride 25 mg/1, phenylephrine hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0067-6095
Product ID
0067-6095_102bd52f-def1-ca60-e063-6294a90a1d4d
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2018-07-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00676095
Hyphenated Format
0067-6095
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
theraflu powerpods nighttime severe cold (source: ndc)
Generic Name
acetaminophen, diphenhydramine hcl, phenylephrine hcl (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 650 mg/1
- 25 mg/1
- 10 mg/1
Packaging
- 8 POUCH in 1 CARTON (0067-6095-01) / 1 POWDER, FOR SOLUTION in 1 POUCH (0067-6095-02)
- 1 POUCH in 1 CARTON (0067-6095-03) / 1 POWDER, FOR SOLUTION in 1 POUCH
Packages (2)
Ingredients (3)
Linked Drug Pages (1)
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"}