YOBISIN

Product NDC: 72988-0012
11-digit product format: 729880012
Labeler code: 72988
Product ID: 72988-0012_0ca8ac22-aaac-9d25-e063-6294a90a4541
Type: HUMAN OTC DRUG
Nonproprietary name: rehmannia root, angelica gigas root
Dosage form: TABLET
Route: ORAL
Labeler: Lydia Co., Ltd.
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2019-04-22
Substance: AKEBIA STEM; ALISMA PLANTAGO-AQUATICA ROOT; ANGELICA GIGAS ROOT; CHINESE CINNAMON; FORSYTHIA SUSPENSA FRUIT; GINGER; LICORICE; PLANTAGO SEED; REHMANNIA GLUTINOSA ROOT; RHUBARB; SCUTELLARIA BAICALENSIS ROOT
Active strength: 416.7; 250; 416.7; 16.7; 16.7; 16.7; 125; 250; 416.7; 16.7; 250 mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1
Pharmacologic classes: Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 8 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	72988-0012-1	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	72988-0012-1	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	72988-0012-1	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded product	product		`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	72988-0012-1	`8dfbde2a14a4…`	`c9ff85d89658…`

Additional Listing Data#

Finished product: Yes
Brand name base: YOBISIN
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
RHUBARB	416.7 mg/1
REHMANNIA GLUTINOSA ROOT	250 mg/1
ANGELICA GIGAS ROOT	416.7 mg/1
AKEBIA STEM	16.7 mg/1
SCUTELLARIA BAICALENSIS ROOT	16.7 mg/1
LICORICE	16.7 mg/1
ALISMA PLANTAGO-AQUATICA ROOT	125 mg/1
FORSYTHIA SUSPENSA FRUIT	250 mg/1
PLANTAGO SEED	416.7 mg/1
GINGER	16.7 mg/1
CHINESE CINNAMON	250 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 11 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
G280W4MW6E	Internal UNII lookup
1BEM3U6LQQ	Internal UNII lookup
32766B2FHX	Internal UNII lookup
531B9G152H	Internal UNII lookup
7J95K7ID2S	Internal UNII lookup
61ZBX54883	Internal UNII lookup
6DXR2088WL	Internal UNII lookup
P4793M1ES5	Internal UNII lookup
9C60Y73166	Internal UNII lookup
C5529G5JPQ	Internal UNII lookup
WS4CQ062KM	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
873ef769-6051-4914-e053-2a95a90a9edb	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72988-0012-1	2023-12-16	C162847	48780-1	ba0f9c33-309f-a910-e053-dadaa90a0b85	Drug Facts
72988-0012-1	2021-01-29	C162847	48780-1	ba0f9c33-309f-a910-e053-dadaa90a0b85	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72988-0012-1	YOBISIN	20 in 1 PACKAGE	TABLET	20		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72988-0012	YOBISIN (REHMANNIA ROOT, ANGELICA GIGAS ROOT) TABLET [LYDIA CO., LTD.]	3	Current NDC, Legacy NDC, 1 package rows	20231217_873ef769-6051-4914-e053-2a95a90a9edb.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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
YOBISIN	REHMANNIA ROOT, ANGELICA GIGAS ROOT	Lydia Co., Ltd.	873ef769-6051-4914-e053-2a95a90a9edb	2023-12-16	Warnings	Exact identifier ndc (product): 72988-0012

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
531B9G152H	AKEBIA STEM		AKEBIA STEM
6DXR2088WL	ALISMA PLANTAGO-AQUATICA ROOT		ALISMA PLANTAGO-AQUATICA ROOT
32766B2FHX	ANGELICA GIGAS ROOT		ANGELICA GIGAS ROOT
WS4CQ062KM	CHINESE CINNAMON		CHINESE CINNAMON
P4793M1ES5	FORSYTHIA SUSPENSA FRUIT		FORSYTHIA SUSPENSA FRUIT
C5529G5JPQ	GINGER		GINGER
61ZBX54883	LICORICE		LICORICE
9C60Y73166	PLANTAGO SEED	8063-16-9	PLANTAGO SEED
1BEM3U6LQQ	REHMANNIA GLUTINOSA ROOT		REHMANNIA GLUTINOSA ROOT
G280W4MW6E	RHUBARB	8016-55-5	RHUBARB
7J95K7ID2S	SCUTELLARIA BAICALENSIS ROOT		SCUTELLARIA BAICALENSIS ROOT

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
72988-0012-1	72988001201	20 TABLET in 1 PACKAGE (72988-0012-1)	20 tablet	2019-04-24	No	No	Current