Seacall Hydrocortisone Ointment.

Product NDC: 76986-006
11-digit product format: 769860006
Labeler code: 76986
Product ID: 76986-006_3616980a-03dd-deba-e063-6394a90a6ce7
Type: HUMAN OTC DRUG
Nonproprietary name: Seacall Hydrocortisone Ointment
Dosage form: OINTMENT
Route: TOPICAL
Labeler: Guangdong Quadrant Ecological Technology Co., Ltd.
Application: M005
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2025-05-27
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

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: Seacall Hydrocortisone Ointment.
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
2714656	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
3616980a-03dc-deba-e063-6394a90a6ce7	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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76986-006-01	Seacall Hydrocortisone Ointment.	20 g in 1 TUBE	OINTMENT	20		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76986-006	SEACALL HYDROCORTISONE OINTMENT. (SEACALL HYDROCORTISONE OINTMENT) OINTMENT [GUANGDONG QUADRANT ECOLOGICAL TECHNOLOGY CO., LTD.]	1	Current NDC, 1 package rows	20250529_3616980a-03dc-deba-e063-6394a90a6ce7.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 49 of 49 · 973 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Evercare Antifungal Treatment Super Absorbent Powder	MICONAZOLE NITRATE	PANEFFORT, LLC	f91910f3-b461-43a4-9120-fda69483fffa	2023-10-26	Warnings	Exact identifier application number: M005
Thera plus Antifungal Clotrimazole	CLOTRIMAZOLE	FOURSTAR GROUP USA, INC.	1265be99-8922-4b76-bd63-19bfb42c3896	2023-10-26	Warnings	Exact identifier application number: M005
Thera plus Antifungal Tolnaftate	TOLNAFTATE	FOURSTAR GROUP USA, INC.	c628dda8-7a6d-5f3a-e053-2995a90a35f8	2023-10-26	Warnings	Exact identifier application number: M005
Povidone Iodine	POVIDONE IODINE	Jianerkang Medical Co., Ltd	e1789944-3a41-4c86-b173-3a6993ae2141	2023-10-23	Warnings	Exact identifier application number: M005
Povidone Iodine Impregnated	POVIDONE IODINE	Jianerkang Medical Co., Ltd	14f2a1dd-92c2-49e8-9fa0-a9d88e8c530d	2023-10-23	Warnings	Exact identifier application number: M005
Povidone Iodine Impregnated	POVIDONE IODINE	Jianerkang Medical Co., Ltd	b82cea56-b09f-411d-a6cf-c53b3ce0e3b6	2023-10-23	Warnings	Exact identifier application number: M005
Povidone Iodine Scrub	POVIDONE-IODINE	Jianerkang Medical Co., Ltd	78131b57-1ffc-4eb8-821e-f7bb73300fe9	2023-10-23	Warnings	Exact identifier application number: M005
Povidone Iodine	POVIDONE IODINE	Jianerkang Medical Co., Ltd	eb30e5de-9074-4760-8e92-e1d1c127227d	2023-10-23	Warnings	Exact identifier application number: M005
Povidone Iodine	POVIDONE IODINE	Jianerkang Medical Co., Ltd	0bd3de76-b726-41f1-87bc-14ab8a1eca8e	2023-10-23	Warnings	Exact identifier application number: M005
Povidone Iodine Prep Pad	POVIDONE-IODINE	Jianerkang Medical Co., Ltd	be85ec5b-eb49-4f1a-a87d-5c9705a20f23	2023-10-22	Warnings	Exact identifier application number: M005
EVERLIT CARE Hand Sanitizer	ETHYL ALCOHOL	Nantong Health & Beyond Hygienic Products Inc.	579c1ab5-50b4-4b5a-a189-c1e2827d0c3a	2023-10-14	Warnings	Exact identifier application number: M005
Micomitin Antifungal	CLOTRIMAZOLE	PureTek Corporation	dd05f5f9-2412-1295-e053-2995a90acb96	2022-02-14	Warnings	Exact identifier application number: M005
Micatin	MICONAZOLE NITRATE	WellSpring Pharmaceutical Corporation	96c56ba1-c3a8-48ce-ab58-550959485e3c	2016-04-07	Warnings	Exact identifier application number: M005

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
2714656	hydrocortisone 0.1 % Topical Ointment	PSN	3616980a-03dc-deba-e063-6394a90a6ce7	1
2714656	hydrocortisone 0.001 MG/MG Topical Ointment	SCD	3616980a-03dc-deba-e063-6394a90a6ce7	1
2714656	hydrocortisone 0.1 % Topical Ointment	SY	3616980a-03dc-deba-e063-6394a90a6ce7	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
76986-006-01	76986000601	20 g in 1 TUBE (76986-006-01)	20 g	2025-05-27	No	No	Current