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.

Identifier, FDA.report destination table
Identifier	FDA.report destination
aa47ff08-07b3-4fd1-bae5-420e4b928f06	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
baf7f49c-75b6-496b-a00e-8e766a8e4f03	Product name	1	20210127
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
ebc62596-fc97-4d03-9483-7ba095d25db7	Product name	1	20151210
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
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
60541-1900-3	2020-01-31	C162847	48780-1	9d75b9d0-43cc-f424-e053-dadaa90a57ce	DRUG FACTS

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 15 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Lidocaine and Menthol	LIDOCAINE AND MENTHOL	Advanced Rx of Tennessee, LLC	44840250-2112-6ef4-e063-6394a90acdcc	2026-06-12	Warnings	Exact identifier application number: M017
DRAWYUM Pain Relief Gel-Patch	LIDOCAINE 4% PAIN RELIEF GEL-PATCH	Jiangxi Yudexi Pharmaceutical Co., LTD	497e6e18-ba46-0001-e063-6294a90af026	2026-06-12	Warnings	Exact identifier application number: M017
NATUHEAL JOINT BACK PAIN RELIEF	ARNICA MONTANA HPUS 7% JOINT BACK PAIN RELIEF	Jiangxi Yudexi Pharmaceutical Co., LTD	4c923afa-4d1e-0776-e063-6294a90a2f54	2026-06-12	Warnings	Exact identifier application number: M017
Hydrocortisone with Aloe	HYDROCORTISONE CREAM 1%	Aldermed Inc.	4a7b532e-b292-b595-e063-6394a90acc9c	2026-06-12	Warnings	Exact identifier application number: M017
MG PLUS MENTHOL	MENTHOL	RENU LABORATORIES, LLC	53737365-b985-3800-e063-6294a90a37f2	2026-06-11	Warnings	Exact identifier application number: M017
CeraVe Developed with Dermatologists Itch Relief Moisturizing	PRAMOXINE HYDROCHLORIDE	L'Oreal USA Products Inc	7c78d980-fc94-498c-aec5-464c0c76c8f4	2026-06-11	Warnings	Exact identifier application number: M017
ANIXIKE Numbing	LIDOCAINE4% NUMBING	Jiangxi Yudexi Pharmaceutical Co., LTD	4a47f1ed-d8cf-3b0b-e063-6394a90a932a	2026-06-11	Warnings	Exact identifier application number: M017
Anti-Itch Soothing Wipes 1 Pramoxine Hydrochloride	PRAMOXINE HYDROCHLORIDE	The Honey Pot Company LLC	81ab7fa7-d9b0-49dc-9782-02f37e588c5e	2026-06-10	Warnings	Exact identifier application number: M017
HealthWise Pain Relief Cream with Lidocaine	LIDOCAINE HYDROCHLORIDE	Veridian Healthcare	ef176d33-10b9-ddb2-e053-2995a90a76e3	2026-06-10	Warnings	Exact identifier application number: M017
Warm Patch Tong Gu Huo Luo Gao	PAIN PATCH	Sheng Chang Pharmaceutical Co, Ltd. Zhongli Factory	6906c4a0-1557-45e3-b915-80e4dd652ee7	2026-06-10	Warnings	Exact identifier application number: M017
LidoMedix	LIDOCAINE, MENTHOL, CAMPHOR	Absolute Therapeutics, LLC	53d504ef-eea3-6a47-e063-6394a90a1f65	2026-06-09	Warnings	Exact identifier application number: M017
good sense anti itch	HYDROCORTISONE	Preferred Pharmaceuticals Inc.	e51047da-8e17-4dd7-be3c-54820a7485f2	2026-06-09	Warnings	Exact identifier application number: M017
Terramed Just Think Comfort GynoCare BV Guard Intimate Wash	PRAMOXINE HYDROCHLORIDE	Rida LLC	09964550-049c-4c3b-817d-37e660c2e45c	2026-06-08	Warnings	Exact identifier application number: M017
Quality Choice Lidocaine Pain Relief Patch	LIDOCAINE	Quality Choice (CHAIN DRUG MARKETING ASSOCIATION)	526abe69-4bbc-6e73-e063-6394a90ad25d	2026-06-08	Warnings	Exact identifier application number: M017
Dcsily Numbing Cream	LIDOCAINE	Shenzhen Xinxin Yunhai Technology Co., Ltd.	53cab09c-6d5d-471e-e063-6294a90aa977	2026-06-08	Warnings	Exact identifier application number: M017
Easment 0.1% Capsaicin cream for sensitive skin	CAPSAICIN 0.1%	Easment LLC	537e0106-9e1c-66b8-e063-6294a90ac538	2026-06-05	Warnings	Exact identifier application number: M017
Maximum Strength Pain Relief	MENTHOL CREAM	OWELL NATURALS LLC	5388f2c5-8cfd-a601-e063-6294a90a2e5f	2026-06-04	Warnings	Exact identifier application number: M017
MG PLUS ROLL ON	MENTHOL ROLL ON	RENU LABORATORIES, LLC	535dc42f-38c7-2afc-e063-6294a90ae23d	2026-06-03	Warnings	Exact identifier application number: M017
OP First Aid Series Insect Sting Relief Pad	BENZOCAINE, ISOPROPYL ALCOHOL	Yiwu Ori-Power Medtech Co.,Ltd.	b43af183-834a-0f64-e053-2995a90a3218	2026-06-03	Warnings	Exact identifier application number: M017
PURE PRIMAL DELAY	LIDOCAINE HCL	Prodigy Media Inc	1ddab664-7c44-452f-854f-e386cd69505e	2026-06-03	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
198706	hydrocortisone 1 % Topical Gel	PSN	aa47ff08-07b3-4fd1-bae5-420e4b928f06	3
198706	hydrocortisone 0.01 MG/MG Topical Gel	SCD	aa47ff08-07b3-4fd1-bae5-420e4b928f06	3
198706	hydrocortisone 1 % Topical Gel	SY	aa47ff08-07b3-4fd1-bae5-420e4b928f06	3

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

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
DRUG FACTS	Hayden Caleel LLC \| Island Kinetics, Inc. d.b.a. CoValence Laboratories	2025-01-05	HUMAN OTC DRUG LABEL	3