head and shoulders scalp x minoxidil hair regrowth treatment for men

Generic: minoxidil

Labeler: the procter & gamble manufacturing company
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name head and shoulders scalp x minoxidil hair regrowth treatment for men
Generic Name minoxidil
Labeler the procter & gamble manufacturing company
Dosage Form SOLUTION
Routes
TOPICAL
Active Ingredients

minoxidil 5 g/100mL

Manufacturer
The Procter & Gamble Manufacturing Company

Identifiers & Regulatory

Product NDC 69423-559
Product ID 69423-559_4744d648-5469-220c-e063-6294a90a3d6c
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA091344
Marketing Start 2023-01-15
Marketing End 2026-05-01

Pharmacologic Class

Established (EPC)
arteriolar vasodilator [epc]
Physiologic Effect
arteriolar vasodilation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69423559
Hyphenated Format 69423-559

Supplemental Identifiers

RxCUI
311724
UNII
5965120SH1
NUI
N0000175379 N0000175564

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 head and shoulders scalp x minoxidil hair regrowth treatment for men (source: ndc)
Generic Name minoxidil (source: ndc)
Application Number ANDA091344 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 5 g/100mL
source: ndc
Packaging
  • 3 BOTTLE, DROPPER in 1 CARTON (69423-559-01) / 60 mL in 1 BOTTLE, DROPPER
source: ndc

Packages (1)

69423-559-01 3 BOTTLE, DROPPER in 1 CARTON (69423-559-01) / 60 mL in 1 BOTTLE, DROPPER

Ingredients (1)

minoxidil (5 g/100mL)

Linked Drug Pages (1)

Head and Shoulders Scalp X Minoxidil Hair Regrowth Treatment for Men ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4744d648-5469-220c-e063-6294a90a3d6c", "openfda": {"nui": ["N0000175379", "N0000175564"], "unii": ["5965120SH1"], "rxcui": ["311724"], "spl_set_id": ["f28f6336-1c3d-769b-e053-2a95a90a3deb"], "pharm_class_pe": ["Arteriolar Vasodilation [PE]"], "pharm_class_epc": ["Arteriolar Vasodilator [EPC]"], "manufacturer_name": ["The Procter & Gamble Manufacturing Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BOTTLE, DROPPER in 1 CARTON (69423-559-01)  / 60 mL in 1 BOTTLE, DROPPER", "package_ndc": "69423-559-01", "marketing_end_date": "20260501", "marketing_start_date": "20230115"}], "brand_name": "Head and Shoulders Scalp X Minoxidil Hair Regrowth Treatment for Men", "product_id": "69423-559_4744d648-5469-220c-e063-6294a90a3d6c", "dosage_form": "SOLUTION", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "69423-559", "generic_name": "Minoxidil", "labeler_name": "The Procter & Gamble Manufacturing Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Head and Shoulders Scalp X Minoxidil Hair Regrowth Treatment for Men", "active_ingredients": [{"name": "MINOXIDIL", "strength": "5 g/100mL"}], "application_number": "ANDA091344", "marketing_category": "ANDA", "marketing_end_date": "20260501", "marketing_start_date": "20230115"}