Home NDC 70484-007 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 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.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# 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 50 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 Ahold U.S.A., Inc, 7e7a813e-424d-4a78-9c72-541c3c62606a 2025-12-28 Warnings Exact identifier application number: M017 Amazon Basics Cold and Hot Medicated Patch MENTHOL Amazon.com Services LLC e3b4db12-c846-b984-e053-2a95a90a8e9a 2025-12-28 Warnings Exact identifier application number: M017 Amazon Basics Pain Relief Patch with 4% Lidocaine LIDOCAINE Amazon.com Services LLC e3b4f9b1-ac6b-cb2a-e053-2a95a90a9e1e 2025-12-28 Warnings Exact identifier application number: M017 Absorbine Jr Neck and Shoulder ABSORBINE JR NECK AND SHOULDER Clarion Brands LLC 22f2f191-9146-3075-e063-6394a90aef5f 2025-12-28 Warnings Exact identifier application number: M017 Absorbine Jr. Pain Relieving Knee Patch ABSORBINE JR. PAIN RELIEVING KNEE PATCH Clarion Brands, LLC 22f71254-e521-2d82-e063-6394a90a12d8 2025-12-28 Warnings Exact identifier application number: M017 Absorbine Jr Back Patch ABSORBINE JR BACK PATCH Clarion Brands LLC. 22f5147e-ff2b-4ae8-e063-6394a90a4e54 2025-12-28 Warnings Exact identifier application number: M017 Absorbine Jr. Pro Rollon ABSORBINE JR. PRO ROLLON Clarion Brands, LLC 470efcd0-d350-3dc4-e063-6394a90ab8c1 2025-12-28 Warnings Exact identifier application number: M017 Med Rub Balm ACHES AND PAIN BALM Wellmetech Pharmaceutical Industries SDN BHD a5801566-6bbe-44f6-8761-9c1ce3096900 2025-12-27 Warnings Exact identifier application number: M017 N-Labs ArcticZen Pain Relief Knee CAMPHOR (SYNTHETIC), MENTHOL Nutriomo Labs PTE., LTD 46e92db7-a48b-2c7a-e063-6394a90a438e 2025-12-27 Warnings Exact identifier application number: M017 Absorbine Jr. Plus MENTHOL Clarion Brands, LLC 46f4ad3c-7418-a6bf-e063-6394a90a4eb8 2025-12-27 Warnings Exact identifier application number: M017 Equate Lidocaine Cool and Heat LIDOCAINE 4% PLUS MENTHOL 1% Walmart Stores Inc b86769c3-a0b4-c481-e053-2a95a90af38b 2025-12-27 Warnings Exact identifier application number: M017 Medicated Body Extra Strength Powder MENTHOL 0.80% Walmart Stores Inc b0786418-7b28-d316-e053-2995a90a3ab5 2025-12-27 Warnings Exact identifier application number: M017 Maximum Strength Medicated Foot Powder MEDICATED FOOT POWDER Walmart Stores Inc b0794d48-eb8b-55c9-e053-2995a90a5b38 2025-12-27 Warnings Exact identifier application number: M017 Walgreens 24-Hour Lidocaine Patch LIDOCAINE 4% Walgreens Company b8402924-b5fc-0acd-e053-2a95a90a1805 2025-12-27 Warnings Exact identifier application number: M017 Frankincense and Myrrh Foot Pain Relief MENTHOL WISE CONSUMER PRODUCTS CO. 115f1abc-34aa-3c20-e063-6294a90a9764 2025-12-26 Warnings Exact identifier application number: M017 Soothing Nerve Relief MENTHOL Wise Consumer Products 46e23c95-1a36-214e-e063-6394a90a98a8 2025-12-26 Warnings Exact identifier application number: M017 Frankincense and Myrrh Foot Pain Relief Combo Pack MENTHOL WISE CONSUMER PRODUCTS CO. 46e2c8b6-bd94-7100-e063-6294a90ac998 2025-12-26 Warnings Exact identifier application number: M017 Pain Patch Perfecto 24 Hours Lidocaine 4 % Patch LIDOCAINE Painpatchperfecto LLC a281c3e9-1c48-4905-98cc-3cedf6042adc 2025-12-25 Warnings Exact identifier application number: M017 Aloe UP SPF 33 Mineral ZINC OXIDE Aloe Care International, LLC 35aa6196-682d-8f32-e063-6394a90aad99 2025-12-24 Warnings Exact identifier application number: M017 ETADERM Numbing Cream LIDOCAINE NUEPHASE LLC 5292c6ff-b878-4e71-878b-4bf08207612e 2025-12-24 Warnings Exact identifier application number: M017
DailyMed RxNorm Mappings# 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