NDC 84067-913 - Hair Loss Growth

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: 84067-913
Package NDCs from labels: 84067-913-01
Manufacturer: Shantou Youjia E-Commerce Co., Ltd.
Effective date: 2024-04-09
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
SOUTH MOON Hair Loss Growth Soap	Shantou Youjia E-Commerce Co., Ltd.	2024-04-09	HUMAN OTC DRUG LABEL

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 10 of 10 · 184 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
YSNORE	DIOSCOREA VILLOSA ROOT, GINGER	Y Snore	4f0a27f1-1584-4bca-b6b8-b5cd273e7242	2018-01-09	Warnings	Exact identifier unii: C5529G5JPQ
H7 Complex	ARNICA MONTANA, CARDUUS MARIANUS, HEPAR SUIS, HYPOPHYSIS SUIS, PANAX GINSENG, PHOSPHORICUM ACIDUM	Maximum Results Solution, Inc.	386fba2d-1523-4e4b-b0ab-7981523c65ab	2017-11-29	Warnings	Exact identifier unii: CUQ3A77YXI
Estrogen and Progesterone	AGNUS CASTUS, ANGELICA SINENSIS, APIS MELLIFICA, ARNICA MONTANA, CIMICIFUGA RACEMOSA, ESTRADIOL, ESTRIOL, FOLLICULINUM, GALIUM APARINE, GLYCYRRHIZA GLABRA, KOREAN GINSENG, OOPHORINUM (SUIS), PROGESTERONE, SEPIA, THUJA OCCIDENTALIS, VISCUM ALBUM	ProBLEN	71fec93b-43b7-4ebb-ab5c-5f544d8e6cbf	2017-01-12	Warnings	Exact identifier unii: CUQ3A77YXI
DNA RNA	ARNICA MONTANA, AVENA SATIVA, DAMIANA, DNA, HYPOPHYSIS SUIS, OLEUM ANIMALE, PANAX GINSENG, RNA, THUJA OCCIDENTALIS	ProBLEN	c7b5d739-2f25-4149-a6e0-efa54293604d	2016-11-23	Warnings	Exact identifier unii: CUQ3A77YXI

Reported adverse events (FAERS/openFDA)#

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