Viatrexx-GI

Product NDC: 63776-189
Requested package NDC: 63776-189-16
11-digit product format: 637760189
Labeler code: 63776
Product ID: 63776-189_e73f8987-8244-4948-adc1-0e9d09497625
Type: HUMAN OTC DRUG
Nonproprietary name: Anti-Interleukin 1, Ankle Articulations, Beta Endorphin, bFGF, Calcaneal tendon, Hip Articulation, Knee Articulation, Liver, Transforming Growth Factor-1, Transforming GF-Beta
Dosage form: SPRAY
Route: ORAL; TOPICAL
Labeler: VIATREXX BIO INCORPORATED
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2019-03-29
Marketing end: 0000-00-00
Substance: ALOE; ALUMINUM OXIDE; BRYONIA ALBA ROOT; MILK THISTLE; CHELIDONIUM MAJUS; COLLINSONIA CANADENSIS ROOT; SUS SCROFA COLON; BOS TAURUS COLON; FRANGULA ALNUS BARK; INTERLEUKIN-12 HUMAN; INTERFERON GAMMA-1A; POTASSIUM CARBONATE; SODIUM CARBONATE; NIACIN; STRYCHNOS NUX-VOMICA SEED; PANTOTHENIC ACID; BOS TAURUS PEYER'S PATCH; SUS SCROFA PEYER'S PATCH; SUS SCROFA RECTUM; SEROTONIN; TARAXACUM OFFICINALE; THIAMINE; VITAMIN D
Active strength: 30 [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	63776-189	63776-189-16	I	Inactivated by FDA		2026-10-05

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 · 16 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	`1332a3947898…`	`d4bfe170f9cd…`
2022-08-30 03:57 UTC · source 2022-08-29	`fb8cb913e6d1…`	`eb8c232b6be0…`

Reported adverse events (FAERS/openFDA)#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
cf050ccd-1144-f76a-e00d-e5698d8597d4	Product name	6	20250625
e2dae634-14ed-febf-08ee-93196433b5b7	Product name	9	20190614
0a5e5249-329b-0cff-e714-77159f193a87	Product name	1	20140508
6b7a6f32-42a6-994d-5ab6-d180e92ee9d8	Product name	1	20140508
d394f843-7479-dc48-dbd3-232266c5548c	Product name	1	20140508
dc9a5fb6-14e2-1cc8-a567-a781fd1f0212	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Related label table
NDC	Related label
63776-189-11	GI
63776-189-14	GI
63776-189-15	GI
63776-189-16	GI
63776-189-17	GI

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
63776-189-11	Viatrexx-GI	0.5 mL in 1 AMPULE	SPRAY	0.5	1
63776-189-11	Viatrexx-GI	1 in 1 BOX	SPRAY	1	1
63776-189-14	Viatrexx-GI	1 in 1 BOX	SPRAY	1	1
63776-189-14	Viatrexx-GI	30 mL in 1 BOTTLE, SPRAY	SPRAY	30	1
63776-189-15	Viatrexx-GI	50 mL in 1 BOTTLE, SPRAY	SPRAY	50	1
63776-189-15	Viatrexx-GI	1 in 1 BOX	SPRAY	1	1
63776-189-16	Viatrexx-GI	1 in 1 BOX	SPRAY	1	1
63776-189-16	Viatrexx-GI	100 mL in 1 BOTTLE	SPRAY	100	1
63776-189-17	Viatrexx-GI	1 in 1 BOX	SPRAY	1	1
63776-189-17	Viatrexx-GI	250 mL in 1 BOTTLE	SPRAY	250	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63776-189	VIATREXX-GI (ANTI-INTERLEUKIN 1, ANKLE ARTICULATIONS, BETA ENDORPHIN, BFGF, CALCANEAL TENDON, HIP ARTICULATION, KNEE ARTICULATION, LIVER, TRANSFORMING GROWTH FACTOR-1, TRANSFORMING GF-BETA) SPRAY [VIATREXX BIO INCORPORATED]	1	Legacy NDC, 10 package rows	20210124_2e8c2a20-69f0-4705-a722-9e40870c8e5b.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
V5VD430YW9	ALOE		ALOE
LMI26O6933	ALUMINUM OXIDE	1344-28-1	ALUMINUM OXIDE
T7J046YI2B	BRYONIA ALBA ROOT		BRYONIA ALBA ROOT
U946SH95EE	MILK THISTLE	65666-07-1	MILK THISTLE
7E889U5RNN	CHELIDONIUM MAJUS		CHELIDONIUM MAJUS
O2630F3XDR	COLLINSONIA CANADENSIS ROOT		COLLINSONIA CANADENSIS ROOT
94J255A0UC	SUS SCROFA COLON		SUS SCROFA COLON
8PD5L21RYS	BOS TAURUS COLON		BOS TAURUS COLON
S2D77IH61R	FRANGULA ALNUS BARK		FRANGULA ALNUS BARK
7B590791ER	INTERLEUKIN-12 HUMAN		INTERLEUKIN-12 HUMAN
VC9M78242P	INTERFERON GAMMA-1A	98059-18-8	INTERFERON GAMMA-1A
BQN1B9B9HA	POTASSIUM CARBONATE	584-08-7	POTASSIUM CARBONATE
45P3261C7T	SODIUM CARBONATE	497-19-8	SODIUM CARBONATE
2679MF687A	NIACIN	59-67-6	NIACIN
269XH13919	STRYCHNOS NUX-VOMICA SEED	8046-97-7	STRYCHNOS NUX-VOMICA SEED
19F5HK2737	PANTOTHENIC ACID	79-83-4	PANTOTHENIC ACID
XB9AHC8DW1	BOS TAURUS PEYER'S PATCH		BOS TAURUS PEYER'S PATCH
308LM01C72	SUS SCROFA PEYER'S PATCH		SUS SCROFA PEYER'S PATCH
QV1358E70N	SUS SCROFA RECTUM		SUS SCROFA RECTUM
333DO1RDJY	SEROTONIN	50-67-9	SEROTONIN
39981FM375	TARAXACUM OFFICINALE		TARAXACUM OFFICINALE
X66NSO3N35	THIAMINE	59-43-8	THIAMINE
9VU1KI44GP	VITAMIN D	1406-16-2	VITAMIN D

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63776-189-16	63776018916	1 BOTTLE in 1 BOX (63776-189-16) > 100 mL in 1 BOTTLE	1 bottle	2019-07-05	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
GI	VIATREXX BIO INCORPORATED \| 8046255 Canada Inc \| Les Importations Herbasante Inc	2019-03-19	HUMAN OTC DRUG LABEL	1