Post-Treatment Repair Cream

Product NDC: 70484-007
11-digit product format: 704840007
Labeler code: 70484
Product ID: 70484-007_37f23f3e-04ca-6fd3-e063-6294a90ac48b
Type: HUMAN OTC DRUG
Nonproprietary name: Hydrocortisone
Dosage form: CREAM
Route: TOPICAL
Labeler: Vi Medical Products Inc.
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2020-06-30
Substance: HYDROCORTISONE
Active strength: 1 g/100mL
Pharmacologic classes: Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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	70484-007	70484-007-01	D	Discontinued by firm		2026-10-21

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 · 34 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	70484-007-01	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	70484-007-01	D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	70484-007-01	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	70484-007-01	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	70484-007-01	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	70484-007-01	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		I	Inactivated by FDA	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	70484-007-01	I	Inactivated by FDA	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		I	Inactivated by FDA	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	70484-007-01	I	Inactivated by FDA	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		I	Inactivated by FDA	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	70484-007-01	I	Inactivated by FDA	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		I	Inactivated by FDA	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	70484-007-01	I	Inactivated by FDA	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		I	Inactivated by FDA	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	70484-007-01	I	Inactivated by FDA	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		I	Inactivated by FDA	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	70484-007-01	I	Inactivated by FDA	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		I	Inactivated by FDA	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	70484-007-01	I	Inactivated by FDA	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		I	Inactivated by FDA	`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	70484-007-01	I	Inactivated by FDA	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		I	Inactivated by FDA	`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	70484-007-01	I	Inactivated by FDA	`1332a3947898…`	`d4bfe170f9cd…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	70484-007-01	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	70484-007-01	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	70484-007-01	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: Post-Treatment Repair Cream
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
HYDROCORTISONE	1 g/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
WI4X0X7BPJ	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
106258	Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
ab8885a9-0778-28ff-e053-2995a90a2e12	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
15bd4439-874a-4934-9954-248e5455d460	Product name	1	20260310
9962b773-9f2e-22cc-0032-535e48ac417b	Product name	3	20250724
56bb0587-1bf2-48b2-9d93-fc9f59d1eeb2	Product name	1	20250325
4d56e8eb-d741-d4a5-de3f-2bab1af75a60	Product name	7	20220608
626d7260-31b5-4412-84fd-579746adb6b3	Product name	1	20210513
8a011600-5e61-4c59-ab7b-54ab658a3b71	Product name	2	20181127
a919621a-248d-3c7a-1084-9f9ce286fdfd	Product name	2	20181009
e7d5a174-836b-a0af-b014-cb0826c69ddc	Product name	2	20181004
fcce390d-6460-4701-87cf-940d8800a1c3	Product name	2	20180212
bf065fa6-1e3b-e4c3-0bde-2dc842ceeea1	Product name	2	20150218
02657a3f-1489-66ea-f740-5ab9524e57d7	Product name	1	20140508
26f3d783-2cc1-4327-e77d-71804cf675a2	Product name	1	20140508
36fdc54c-bbeb-981e-8a53-4d768e283892	Product name	1	20140508
58f3f9b7-3b9b-a9c1-1c9f-18ac777192b8	Product name	1	20140508
61e59a42-186b-9f4b-aec3-fb49a6debc31	Product name	1	20140508
705740e1-dee5-2610-c5a3-4c59cd9d62af	Product name	1	20140508
7bdc4804-3832-c0df-e519-72b6d47c9792	Product name	1	20140508
a7051cba-790b-a699-81f8-dbbbdbd9b5ac	Product name	1	20140508
abaf203f-619e-f265-559f-8c81af5cb1c2	Product name	1	20140508
acc4d8bb-0e29-e9f8-65f8-31e94184a9c0	Product name	1	20140508
b045ad64-0f28-9a02-2f9b-b34d94fb2278	Product name	1	20140508
bfd28ffb-d550-3fe9-f65b-10bcb7f971fd	Product name	1	20140508
da108d9e-edc8-17a3-8c28-3251c6a8accc	Product name	1	20140508
fe21f3fd-a378-0654-1972-db3c3b64470e	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70484-007-01	2025-07-24	C162847	48780-1	d6a99b39-456e-a426-e053-dadaa90af4c2	Post-Treatment Repair Cream
70484-007-01	2022-01-28	C162847	48780-1	d6a99b39-456e-a426-e053-dadaa90af4c2	Post-Treatment Repair Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70484-007-01	Post-Treatment Repair Cream	30 mL in 1 BOTTLE	CREAM	30		2
70484-007-02	Post-Treatment Repair Cream	22 mL in 1 BOTTLE	CREAM	22		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70484-007	POST-TREATMENT REPAIR CREAM (HYDROCORTISONE) CREAM [VI MEDICAL PRODUCTS INC.]	1	Current NDC, Legacy NDC, 2 package rows	20200814_ab8885a9-0778-28ff-e053-2995a90a2e12.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 79 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
PAIN RELIEF PATCHES	LIDOCAINE	Amerisource Bergen	614f1e56-891f-4620-be10-0c075a1dbc3f	2025-09-11	Warnings	Exact identifier application number: M017
Industrial Itch and Pain Relief	DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE	R & R Lotion, Inc	236415fc-f923-4a82-b54a-ecaf666dd2e0	2025-09-11	Warnings	Exact identifier application number: M017
Eco Lips Menthol Medicated Lip Balm	MENTHOL	Eco Lips, Inc.	fc4c25d6-6109-dfd8-e053-6394a90a4e91	2025-09-10	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE 1%	Encube Ethicals, Inc.	d6f5c0df-6262-4704-bb24-430f66bb2ca8	2025-09-09	Warnings	Exact identifier application number: M017
Blue-Emu Lidocaine Pain Relief Cream	LIDOCAINE CREAM 4%	Kingsway Pharmaceuticals dba NFI, LLC	592811f2-e21c-6a58-e053-2991aa0a69a9	2025-09-09	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE	Unifirst First Aid Corporation	282ed5ef-8c2a-4092-9d99-1a7eee7a39e3	2025-09-09	Warnings	Exact identifier application number: M017
LubeLife Climax Control Delay	BENZOCAINE	CC Wellness LLC	e1a98e6d-0c24-75b8-e053-2a95a90ad136	2025-09-09	Warnings	Exact identifier application number: M017
Blue-Emu Maximum Pain Relief	TROLAMINE SALICYLATE	Kingsway Pharmaceuticals dba NFI, LLC	c863351a-951b-4f7c-a9c0-4289d702054a	2025-09-09	Warnings	Exact identifier application number: M017
Tiger Balm Neck and Shoulder Rub	CAMPHOR (SYNTHETIC) AND MENTHOL	Haw Par Healthcare Ltd.	02a65b25-78b2-4e29-9484-40e2228fb384	2025-09-09	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE	Unifirst First Aid Corporation	e90df2e5-2ef4-47dd-bd74-be9cea6d9d85	2025-09-08	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE	Unifirst First Aid Corporation	69d6645e-db3c-4dc0-a9a5-e2bc963e2f28	2025-09-08	Warnings	Exact identifier application number: M017
SupreH Arnica Bruise Cream	SUPREH ARNICA REMEDY PLUS BRUISE CREAM	Shenzhen Xinxin Yunhai Technology Co., Ltd.	3e41fc0e-54c3-2622-e063-6294a90a13c9	2025-09-07	Warnings	Exact identifier application number: M017
Menthol	MENTHOL	FlexiGo Inc	3607c326-6db0-a2cd-e063-6394a90a9eb6	2025-09-06	Warnings	Exact identifier application number: M017
TIDL PAIN RELIEF CRYOTHERAPY MENTHOL Cream	PAIN RELIEF CRYOTHERAPY MENTHOL CREAM	Shenzhen Sam Technology Co., Ltd.	3e08cc87-2385-0838-e063-6394a90abf9b	2025-09-05	Warnings	Exact identifier application number: M017
TIDL CLINICAL CRYOTHERAPY MENTHOL Cream	CLINICAL CRYOTHERAPY MENTHOL CREAM	Shenzhen Sam Technology Co., Ltd.	3e090b98-1db7-4174-e063-6394a90aa539	2025-09-05	Warnings	Exact identifier application number: M017
ALCEMISTE	LIDOCAINE HCL	Price Team Ventures, LLC	4383faaa-49cf-47b7-83a6-c2a94b6ff9b5	2025-09-05	Warnings	Exact identifier application number: M017
Lansinoh Pain Relieving	LIDOCAINE HCL	Lansinoh Laboratories Inc	b7cf1fdb-946d-a4e8-e053-2995a90a26a8	2025-09-05	Warnings	Exact identifier application number: M017
Sumifun PLANTAR RELIEF ROLL -ON	4% LIDOCAINE, 1% MENTHOL	Guangzhou Zhupuyou E-commerce Co., Ltd	3c9ee60b-548a-979f-e063-6394a90a70b0	2025-09-03	Warnings	Exact identifier application number: M017
Meijer Capsaicin Heat Patch	CAPSAICIN	Meijer Distribution	3c465557-0a4f-fb72-e063-6294a90a1ef2	2025-09-02	Warnings	Exact identifier application number: M017
Cold Therapy	MENTHOL	AHC Ventures Corp DBA Cryoderm	dd95c682-8ddf-43e7-a277-2fca6ec744cc	2025-09-02	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
WI4X0X7BPJ	HYDROCORTISONE	50-23-7	HYDROCORTISONE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
106258	hydrocortisone 1 % Topical Cream	PSN	ab8885a9-0778-28ff-e053-2995a90a2e12	2
106258	hydrocortisone 10 MG/ML Topical Cream	SCD	ab8885a9-0778-28ff-e053-2995a90a2e12	2
106258	hydrocortisone 1 % (as hydrocortisone acetate 1.2 % ) Topical Cream	SY	ab8885a9-0778-28ff-e053-2995a90a2e12	2
106258	hydrocortisone 1 % Topical Cream	SY	ab8885a9-0778-28ff-e053-2995a90a2e12	2
106258	hydrocortisone 1 GM per 100 GM Topical Cream	SY	ab8885a9-0778-28ff-e053-2995a90a2e12	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
70484-007-01	70484000701	30 mL in 1 BOTTLE (70484-007-01)	30 ml	2020-08-04	0000-00-00	No	No	Current
70484-007-02	70484000702	22 mL in 1 BOTTLE (70484-007-02)	22 ml	2025-06-30		No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Post-Treatment Repair Cream	Vi Medical Products Inc. \| Vege Labs LLC	2025-06-19	HUMAN OTC DRUG LABEL	2