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 96 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
CVS Pain Relief	MENTHOL 10.5%	CVS	d0ea80ce-38b2-acde-e053-2995a90a47e5	2025-03-31	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE	A2A Integrated Pharmaceuticals, LLC	31431866-6fb5-2acd-e063-6294a90ac520	2025-03-31	Warnings	Exact identifier application number: M017
Citrus Cleansing Foot Soak and Body Soak	CAMPHOR	SANSAR, LLC	f136616d-9f32-4e55-a495-b7466fd68526	2025-03-28	Warnings	Exact identifier application number: M017
Zpol ULTRA	MENTHOL, METHYL SALICYLATE	Laboratorios Zepol S.A.	1a1433a6-8d04-96df-e063-6394a90a987b	2025-03-27	Warnings	Exact identifier application number: M017
Muscle Recovery Foot Soak and Body Soak	CAMPHOR	SANSAR, LLC	1c347267-b653-41bf-9967-7feff17c38af	2025-03-27	Warnings	Exact identifier application number: M017
Soothing Lavender Foot Soak and Body Soak	CAMPHOR	SANSAR, LLC	ef26523a-b2f2-466e-89ad-f293cd64decb	2025-03-27	Warnings	Exact identifier application number: M017
Achelon Lidocaine Patch	LIDOCAINE PATCH 4%	Achelon, Inc	31408e21-e58d-6db5-e063-6294a90aa4bc	2025-03-26	Warnings	Exact identifier application number: M017
Achelon Lidocaine Patch	LIDOCAINE PATCH 4%	Achelon, Inc	3143bb72-2969-d66e-e063-6294a90a4604	2025-03-26	Warnings	Exact identifier application number: M017
Parche Leon	CAPSAICIN, CAMPHOR, MENTHOL	Pharmadel LLC	a8f266fa-6e43-559e-e053-2995a90a2c75	2025-03-26	Warnings	Exact identifier application number: M017
Adellina Numbing Cream	LIDOCAINE	Guangzhou Haishi Biological Technology Co., Ltd.	314a83fe-8bdb-766f-e063-6294a90a61c6	2025-03-26	Warnings	Exact identifier application number: M017
HealthWise Lidocaine Plus Menthol Patch	LIDOCAINE AND MENTHOL	Veridian Healthcare	312f15fe-9297-2dc2-e063-6294a90a6f4d	2025-03-25	Warnings	Exact identifier application number: M017
HealthWise Lidocaine Patch	LIDOCAINE 4%	Veridian Healthcare	3130729d-1679-90cd-e063-6294a90a21e6	2025-03-25	Warnings	Exact identifier application number: M017
HealthWise Lidocaine Patch	LIDOCAINE 4%	Veridian Healthcare	31314dda-6199-574d-e063-6394a90aae7a	2025-03-25	Warnings	Exact identifier application number: M017
RWSEFK Lidocaine Pain Relief Gel-Patch	LIDOCAINE PAIN RELIEF GEL-PATCH	Henan Enokon Medical Instrument Co., Ltd.	31366793-f8a6-a2c4-e063-6294a90acbfc	2025-03-25	Warnings	Exact identifier application number: M017
Forticept Wounds and Burns Hydrogel	BENZETHONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE	Lidan, inc.	c6f58b63-9838-4ff4-8b1a-de2d41d6cf5f	2025-03-25	Warnings	Exact identifier application number: M017
MQ Pain Relieving Patch	PAIN RELIEVING PATCH	Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd	0978ff22-c357-e266-e063-6394a90a98a4	2025-03-24	Warnings	Exact identifier application number: M017
LidoPro Patch (Lidocaine 4%, Menthol 1%)	LIDOCAINE AND MENTHOL PATCH	Advanced Rx of Tennessee, LLC	30c97646-db06-df84-e063-6394a90a7743	2025-03-20	Warnings	Exact identifier application number: M017
Carmex Classic Lip Balm Medicated	CAMPHOR (SYNTHETIC), PETROLATUM	Carma Laboratories, Inc.	fb6eb93b-7dc0-4b6f-bfe1-1a7b47588e57	2025-03-20	Warnings	Exact identifier application number: M017
Carmex Variety Pack Classic Medicated Lip Balm Daily Care Lip Balm SPF	CAMPHOR (SYNTHETIC), WHITE PETROLATUM OCTINOXATE, OXYBENZONE, AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Carma Laboratories, Inc.	5f904369-5f21-4907-98de-df23bce30823	2025-03-20	Warnings	Exact identifier application number: M017
DermaCort Anti-itch	HYDROCORTISONE	Melaleuca, Inc.	24044b0f-dd1e-4762-82b8-7a28b08c2f77	2025-03-20	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