Home NDC 60541-1900 glo SKIN BEAUTY Remedy Gel
Product NDC 60541-1900
11-digit product format 605411900
Labeler code 60541
Product ID 60541-1900_2af7cc72-4838-9f49-e063-6294a90a7adc
Type HUMAN OTC DRUG
Nonproprietary name glo SKIN BEAUTY Remedy Gel
Dosage form GEL
Route TOPICAL
Labeler Hayden Caleel LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-12-31
Substance HYDROCORTISONE
Active strength 1 g/100g
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 · 26 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 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 60541-1900-3 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 60541-1900-3 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 60541-1900-3 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 60541-1900-3 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 60541-1900-3 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 60541-1900-3 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 60541-1900-3 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 60541-1900-3 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 60541-1900-3 I Inactivated by FDA bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 60541-1900-3 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 60541-1900-3 I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 60541-1900-3 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 excluded product product E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 60541-1900-3 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
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 glo SKIN BEAUTY Remedy Gel
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HYDROCORTISONE 1 g/100g
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 198706 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 60541-1900-3 glo SKIN BEAUTY Remedy Gel 1 in 1 CARTON GEL 1 3 60541-1900-3 glo SKIN BEAUTY Remedy Gel 30 g in 1 BOTTLE GEL 30 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 60541-1900 GLO SKIN BEAUTY REMEDY GEL GEL [HAYDEN CALEEL LLC] 3 Current NDC, Legacy NDC, 2 package rows 20250107_aa47ff08-07b3-4fd1-bae5-420e4b928f06.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 62 of 152 · 3,029 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Itch Eraser Gel DIPHENHYDRAMINE HCL Tender Corporation d/b/a Adventure Ready Brands 223c7cfd-6dc5-140a-e063-6394a90a8332 2025-11-17 Warnings Exact identifier application number: M017 Calamine Plus Pramoxine HCl CALAMINE PLUS SPRAY Kroger Co. 6b3e7aac-395f-48cf-9c5e-f7e163724aef 2025-11-17 Warnings Exact identifier application number: M017 Calamine Plus Pramoxine HCl CALAMINE PLUS SPRAY HY-VEE, INC 415ecfe9-3145-f23e-e063-6394a90adfd8 2025-11-17 Warnings Exact identifier application number: M017 AY BENDITO - CBD CAMPHOR, MENTHOL AY BENDITO INTERNATIONAL, INC 04b1d605-60aa-56f4-e063-6294a90ae760 2025-11-17 Warnings Exact identifier application number: M017 AY BENDITO - CBD CAMPHOR, MENTHOL AY BENDITO INTERNATIONAL, INC 0f1406fe-3a2f-bf36-e063-6294a90a7e5e 2025-11-17 Warnings Exact identifier application number: M017 AY BENDITO CBD MENTHOL, CAMPHOR AY BENDITO INTERNATIONAL, INC 30a1c6b7-e37e-32c2-e063-6394a90aa354 2025-11-17 Warnings Exact identifier application number: M017 ETERNAL SPIRIT BEAUTY PAINLESS WITH CBD 3000 MENTHOL, CAMPHOR Worldwide Cosmetics, Inc 0816cc8f-8d0b-de27-e063-6294a90a8a9d 2025-11-17 Warnings Exact identifier application number: M017 JUST CBD ROLL-ON COOLING MENTHOL Just Brands LLC f6538e3e-4663-679c-e053-2995a90a87b5 2025-11-17 Warnings Exact identifier application number: M017 JUST CBD ROLL-ON WARMING CAMPHOR Just Brands LLC f65455d7-04a9-6217-e053-2995a90a7c90 2025-11-17 Warnings Exact identifier application number: M017 JUST CBD - CBD AND THC ULTRA RELIEF MENTHOL, CAMPHOR Just Brands LLC f664eb79-8897-3a49-e053-2995a90a37b4 2025-11-17 Warnings Exact identifier application number: M017 JUST CBD RELIEF SOOTHING LIDOCAINE HCL Just Brands LLC f9aff6e7-5702-f61c-e053-6294a90aa66f 2025-11-17 Warnings Exact identifier application number: M017 JUST CBD SOOTHING MENTHOL, CAMPHOR Just Brands LLC 0abece07-976c-4881-e063-6294a90a5c1b 2025-11-17 Warnings Exact identifier application number: M017 Blue-Emu Thrive Pain Relief Cream TRIPELENNAMINE 0.5% Kingsway Pharmaceuticals dba NFI, LLC a4ba6787-c99b-4bf2-9f8f-e923ef976212 2025-11-14 Warnings Exact identifier application number: M017 CVS Cooling Patch MENTHOL CVS Pharmacy 42d97e29-f32d-a31b-e063-6394a90a88d8 2025-11-14 Warnings Exact identifier application number: M017 Lidocaine LIDOCAINE Marlex Pharmaceuticals Inc 4de2bc60-dc4a-4417-984f-eabab0e926a6 2025-11-14 Warnings Exact identifier application number: M017 EXTREME EMU MENTHOL, METHYL SALICYLATE Renu Laboratories, LLC 4393b57b-1e70-b8dd-e063-6294a90ae748 2025-11-14 Warnings Exact identifier application number: M017 4x Medicated Toothache and Gum Cream BENZOCAINE Kroger a8c5090a-24f9-4e73-e053-2a95a90acca0 2025-11-14 Warnings Exact identifier application number: M017 PM Toothache Relief BENZOCAINE CVS 0a5a8cd0-d680-8a0f-e063-6294a90aa65c 2025-11-14 Warnings Exact identifier application number: M017 PM Toothache Relief BENZOCAINE Walgreens e816f742-fba9-3c12-e053-2a95a90a192f 2025-11-14 Warnings Exact identifier application number: M017 4x Medicated Toothache and Gum Cream BENZOCAINE Walgreens a71c2092-4ece-b82e-e053-2995a90ac933 2025-11-14 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 Sample Exclude flag Status 60541-1900-3 60541190003 1 BOTTLE in 1 CARTON (60541-1900-3) / 30 g in 1 BOTTLE 1 bottle 2017-12-31 No No Current