Trivix

Product NDC: 72275-709
Requested package NDC: 72275-709-77
11-digit product format: 722750709
Labeler code: 72275
Product ID: 72275-709_8f64204b-1bce-2ee0-e053-2995a90af8c7
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Triamcinolone Acetonide Cream .1%, Dimethicone 5% Cream
Dosage form: KIT
Labeler: Primary Pharmaceuticals, Inc.
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2019-08-01
Marketing end: 0000-00-00
Active strength: 0
NDC exclude flag: No
Listing certified through: 2020-12-31
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	72275-709	72275-709-77	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 · 15 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…`

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
16a2c1cd-ae95-d910-f03d-7e06b11dd243	Product name	5	20260202
d4d7da1a-7fd4-628e-cdae-89e749b1c534	Product name	7	20260127
75f7e47b-8736-a182-fc44-22aca8d79689	Product name	2	20251211
653485de-0601-41e4-82db-7a60bb223e27	Product name	1	20251024
62986c8d-91f1-b1ba-b5a3-8b54b75bb8c2	Product name	6	20250516
ef9a935e-31b7-402c-a66c-716cdfe4f126	Product name	9	20241218
23fb3cda-2b50-f3d3-ebde-f542350bd77b	Product name	4	20240828
e42f429b-c4e5-0402-e1c5-730154df4060	Product name	4	20240205
081b54f0-4545-48b6-b854-03e1401f09ea	Product name	1	20230112
38d4de13-64b3-4057-b91c-4b5126962341	Product name	1	20220516
115c5bd2-98e1-4a98-8292-90803ca7e851	Product name	1	20220127
089e0644-1ea8-8654-4113-39f960dd57d5	Product name	3	20210115
1629e00f-54fb-4a43-8306-b58442b23902	Product name	9	20200430
5331c9c8-f64b-11e6-ccf1-071c477fcb0b	Product name	7	20190612
aead65a2-216e-4ff8-a178-44aab77c24ed	Product name	1	20180531
9f64e0dc-109c-9660-8e0e-91ec987b3817	Product name	6	20171204
dfa879a3-32de-49f0-a7ba-9b9c3e13002f	Product name	1	20171204
8de20f81-8411-4cf1-a8b2-03404ee56d01	Product name	3	20171109
a5f1a68c-0352-4f34-46a3-9b4eed239ed8	Product name	2	20160819
ebc62596-fc97-4d03-9483-7ba095d25db7	Product name	1	20151210
355b2224-0895-7135-83f5-d099a6a82a0a	Product name	1	20140508
55be6b50-8cc0-f0f1-74a1-3416a91193aa	Product name	1	20140508
60c52429-fcef-eb54-2387-43bc9e4f296b	Product name	1	20140508
7a0092d1-1e8c-0d78-4f8d-d95fa15cc3cf	Product name	1	20140508
89b93c13-4be8-69f3-b33b-63e64feffb9b	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72275-709-77	2023-01-30	C162847	48780-1	f386c649-e502-0266-e053-dadaa90a7c1a	Trivix

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
53329-152-44	Trivix	118 mL in 1 TUBE	CREAM	118 mL	5 g in 100mL	1
72275-709-77	Trivix	1 in 1 CARTON	KIT	1		1

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
72275-709-77	EA - Each	72275-709	290f1e09-24b4-44b3-b97f-3e533ba5ea06	1	2020-04-20

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72275-709	TRIVIX (TRIAMCINOLONE ACETONIDE CREAM .1%, DIMETHICONE 5% CREAM) KIT [PRIMARY PHARMACEUTICALS, INC.]	1	Legacy NDC, 2 package rows	20190925_8f64204b-1bcd-2ee0-e053-2995a90af8c7.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
259090	dimethicone 5 % Topical Cream	PSN	8f64204b-1bcd-2ee0-e053-2995a90af8c7	1
1014314	triamcinolone acetonide 0.1 % Topical Cream	PSN	8f64204b-1bcd-2ee0-e053-2995a90af8c7	1
259090	dimethicone 50 MG/ML Topical Cream	SCD	8f64204b-1bcd-2ee0-e053-2995a90af8c7	1
1014314	triamcinolone acetonide 1 MG/ML Topical Cream	SCD	8f64204b-1bcd-2ee0-e053-2995a90af8c7	1
259090	dimethicone 5 % Topical Cream	SY	8f64204b-1bcd-2ee0-e053-2995a90af8c7	1
1014314	triamcinolone acetonide 0.1 % Topical Cream	SY	8f64204b-1bcd-2ee0-e053-2995a90af8c7	1
1014314	triamcinolone acetonide 1 MG per GM Topical Cream	SY	8f64204b-1bcd-2ee0-e053-2995a90af8c7	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
72275-709-77	72275070977	1 KIT in 1 CARTON (72275-709-77) * 80 g in 1 TUBE * 118 mL in 1 TUBE (53329-152-44)	1 kit	2019-08-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Trivix	Primary Pharmaceuticals, Inc. \| Biomed Laboratories, LLC. \| Perrigo Israel Pharmaceuticals LTD. \| Rainbow Gold	2019-08-05	HUMAN PRESCRIPTION DRUG LABEL	1