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		2026-10-23

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 117 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MYCO Clinic Pain Relief	MENTHOL	Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions	604a30c9-2306-47a1-bd31-94b63639dd90	2024-11-20	Warnings	Exact identifier application number: M017
MYCO Clinic Pain Relief	CAMPHOR, MENTHOL	Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions	0b489420-3b5c-43c5-aab4-0e3720acf9ce	2024-11-20	Warnings	Exact identifier application number: M017
MYCO Clinic Pain Relief	CAMPHOR, MENTHOL	Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions	dd906129-a787-4352-856d-d7a915031a6e	2024-11-20	Warnings	Exact identifier application number: M017
Walgreens Arthritis Pain Relief Cream	HISTAMINE DIHYDROCHLORIDE	Walgreens Company	80d3031a-7fa9-4f5b-b85e-c7c6ef314801	2024-11-20	Warnings	Exact identifier application number: M017
Anti-Itch Medicated Maximum Strength	BENZOCAINE AND RESORCINOL	Walgreens Company	7fd86dcb-edef-4d0d-b389-7ecea595fe67	2024-11-20	Warnings	Exact identifier application number: M017
Walgreens Pain Relief	BENZOCAINE	Walgreens Company	7cee7234-32cd-4bf3-8a6c-0882585eec7f	2024-11-20	Warnings	Exact identifier application number: M017
Walgreens Advanced Scar Gel	ADVANCED SCAR GEL	Walgreens Company	2c040475-a124-485c-933e-66b452f5ab46	2024-11-20	Warnings	Exact identifier application number: M017
LidoPro Pain Relief	CAPSAICIN AND LIDOCAINE	Clinic Pharma	274611ea-7fc2-ba3f-e063-6294a90aa50f	2024-11-19	Warnings	Exact identifier application number: M017
First Aid Only Sting Relief Pad	BENZOCAINE	Acme United Corporation	5087cbbd-1bbe-62ed-e054-00144ff8d46c	2024-11-19	Warnings	Exact identifier application number: M017
Sting Relief Pad	BENZOCAINE, ISOPROPYL ALCOHOL	Acme United Corporation	6bb9a782-2394-4c8c-e053-2991aa0a08d4	2024-11-19	Warnings	Exact identifier application number: M017
First Aid Only Sting Relief	BENZOCAINE	Acme United Corporation	697127d1-c02e-16d2-e053-2a91aa0a39fd	2024-11-19	Warnings	Exact identifier application number: M017
First Aid Only Hydrocortisone 1% Anti-Itch	HYDROCORTISONE	Acme United Corporation	e5597b11-b08e-99e1-e053-2a95a90a15a5	2024-11-19	Warnings	Exact identifier application number: M017
Equate Cold Therapy Pain Relieving Roll-on Analgesic	MENTHOL, UNSPECIFIED FORM	Wal-Mart Stores, Inc.	4115f0ac-e12a-4e59-94f5-a47dcc7f8766	2024-11-18	Warnings	Exact identifier application number: M017
Equate Cold Therapy Pain Relieving Analgesic	MENTHOL, UNSPECIFIED FORM	Wal-Mart Stores, Inc.	ac6c2112-8692-4628-97d8-3a5a9f509766	2024-11-18	Warnings	Exact identifier application number: M017
Equate Odor-Free Therapy Arthritis Analgesic	TROLAMINE SALICYLATE	Wal-Mart Stores, Inc.	1d73e7b6-c7f9-4680-b3e3-a954b91e1863	2024-11-18	Warnings	Exact identifier application number: M017
First Aid Only Burn	LIDOCAINE HYDROCHLORIDE	Acme United Corporation	9af39fcd-0a57-26d0-e053-2a95a90a99a0	2024-11-17	Warnings	Exact identifier application number: M017
First Aid Only First Aid/Burn	LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE	Acme United Corporation	caa67a05-bdbd-c380-e053-2995a90a0bf1	2024-11-17	Warnings	Exact identifier application number: M017
Meijer Pain Lidocaine Plus Relieving Analgesic	BENZYL ALCOHOL AND LIDOCAINE HYDROCHLORIDE	Meijer Distribution, Inc	b7385140-3f63-4cbc-b557-de1d29d1ea36	2024-11-15	Warnings	Exact identifier application number: M017
Signature Care Hydrocortisone	HYDROCORTISONE	Safeway	c6b9c4e1-bab8-490d-8c00-c43377ad0857	2024-11-15	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE	Walgreen Company	1a9b8b4c-3e15-49e6-af91-76ed0dc0829e	2024-11-15	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