NDC 84232-016-01 - Hair Regen - Hair Regrowth Treatment

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
84232-016
Requested NDC
84232-016-01
Package NDCs from labels
84232-016-01, 84232-016-21
Manufacturer
Yiwu Yizhou Trading Co., Ltd
Effective date
2025-04-15
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Hair Regen - Hair Regrowth Treatment - Yiwu Yizhou Trading Co., LtdYiwu Yizhou Trading Co., Ltd2025-04-15HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84232-016-01Hair Regen - Hair Regrowth Treatment28.35 g in 1 BOTTLE, DISPENSINGAEROSOL, FOAM28.351
84232-016-21Hair Regen - Hair Regrowth Treatment1 in 1 BOXAEROSOL, FOAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84232-016HAIR REGEN - HAIR REGROWTH TREATMENT (WOMENS FOAM MINOXIDIL 1 PK) AEROSOL, FOAM [YIWU YIZHOU TRADING CO., LTD]1Current NDC, 2 package rows20250416_32ba9c8b-3af0-0731-e063-6294a90aa7b4.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 180 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
CVS Hand SanitizerALCOHOLCVSd0081c50-c0d2-436a-ba83-5d1982ae64b72015-08-17WarningsExact identifier
unii: 3K9958V90M
Instant Hand SanitizerALCOHOLSafetec of America, Inc.f9e30645-491b-4f54-acfd-f863ee2356072013-08-07WarningsExact identifier
unii: 3K9958V90M

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.