Shopko

Product NDC: 37012-018
11-digit product format: 370120018
Labeler code: 37012
Product ID: 37012-018_39f985fe-8cfb-9177-e063-6394a90a41b1
Type: HUMAN OTC DRUG
Nonproprietary name: Hydrocortisone
Dosage form: OINTMENT
Route: TOPICAL
Labeler: Shopko Stores Operating Co., LLC
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 1989-10-03
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 · 24 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	37012-018-02	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	37012-018-02	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	37012-018-02	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	37012-018-02	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	37012-018-02	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	37012-018-02	`1332a3947898…`	`d4bfe170f9cd…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	37012-018-02	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	37012-018-02	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	37012-018-02	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded product	product		`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	37012-018-02	`8dfbde2a14a4…`	`c9ff85d89658…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded product	product		`e2bbac7714bc…`	`27bdfed8d636…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded package	package	37012-018-02	`e2bbac7714bc…`	`27bdfed8d636…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded product	product		`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	37012-018-02	`9bebd1f3094a…`	`5416666fcb17…`

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: Shopko
Brand name suffix: Hydrocortisone
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
203105	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
92bcbde3-401a-4301-854e-c352852317d6	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
37012-018-02	2024-11-14	C162847	48780-1	9d75b9d0-2371-f424-e053-dadaa90a57ce	Shopko ® Hydrocortisone
37012-018-02	2020-01-31	C162847	48780-1	9d75b9d0-2371-f424-e053-dadaa90a57ce	Shopko ® Hydrocortisone

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
37012-018-02	ShopkoHydrocortisone	1 in 1 CARTON	OINTMENT	1		3
37012-018-02	ShopkoHydrocortisone	28.4 g in 1 TUBE	OINTMENT	28.4		3

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Hydrocortisone	ACTIVE INGREDIENT	WI4X0X7BPJ	SHOPKO HYDROCORTISONE (HYDROCORTISONE) OINTMENT [SHOPKO STORES OPERATING CO., LLC]	1
Hydrocortisone	ACTIVE MOIETY	WI4X0X7BPJ	SHOPKO HYDROCORTISONE (HYDROCORTISONE) OINTMENT [SHOPKO STORES OPERATING CO., LLC]	1
Medium-chain triglycerides	INACTIVE INGREDIENT	C9H2L21V7U	SHOPKO HYDROCORTISONE (HYDROCORTISONE) OINTMENT [SHOPKO STORES OPERATING CO., LLC]	1
Methylparaben	INACTIVE INGREDIENT	A2I8C7HI9T	SHOPKO HYDROCORTISONE (HYDROCORTISONE) OINTMENT [SHOPKO STORES OPERATING CO., LLC]	1
Petrolatum	INACTIVE INGREDIENT	4T6H12BN9U	SHOPKO HYDROCORTISONE (HYDROCORTISONE) OINTMENT [SHOPKO STORES OPERATING CO., LLC]	1
Propylparaben	INACTIVE INGREDIENT	Z8IX2SC1OH	SHOPKO HYDROCORTISONE (HYDROCORTISONE) OINTMENT [SHOPKO STORES OPERATING CO., LLC]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
37012-018	SHOPKO HYDROCORTISONE (HYDROCORTISONE) OINTMENT [SHOPKO STORES OPERATING CO., LLC]	2	Current NDC, Legacy NDC, 2 package rows	20241116_92bcbde3-401a-4301-854e-c352852317d6.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 16 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Mineral Ice Extreme Dry Stick	MENTHOL	Carlin Consumer Health LLC	4f81be91-92e5-1205-e063-6394a90a6e82	2026-06-02	Warnings	Exact identifier application number: M017
Kalaya Extra Strength Pain Relief Gel with Arnica	METHYL SALICYLATE, MENTHOL, CAMPHOR	Avaria Health & Beauty Corp	b6a6237d-b471-4102-b5df-fc389f5f9258	2026-06-02	Warnings	Exact identifier application number: M017
Biofreeze Ultraflex	LIDOCAINE	Reckitt Benckiser LLC	2655974b-a67d-9f07-e063-6294a90a54e8	2026-06-02	Warnings	Exact identifier application number: M017
Biofreeze Ultraflex Plus	LIDOCAINE, MENTHOL	Reckitt Benckiser LLC	401e1843-e9a6-fda9-e063-6294a90a3073	2026-06-02	Warnings	Exact identifier application number: M017
Pain Relief	MENTHOL SPRAY	Owell Naturals Brand, LLC	534c871c-da35-6135-e063-6294a90aa9f6	2026-06-02	Warnings	Exact identifier application number: M017
Charm Tex FLUORIDE Gel	SODIUM FLUORIDE	Jiangsu Gold Worldworks Household Chemicals Co., Ltd.	09d47bd7-1438-4ef2-85e0-9cd5eb2f763a	2026-05-31	Warnings	Exact identifier application number: M017
Charm Tex FLUORIDE	SODIUM MONOFLUOROPHOSPHATE	Jiangsu Gold Worldworks Household Chemicals Co., Ltd.	2bddc69a-0c0f-47fc-bc98-90c2ec70dd6f	2026-05-31	Warnings	Exact identifier application number: M017
Sting Relief Prep Pad	BENZOCAINE	NINGBO TIANBO FIRST AID PRODUCT CO., LTD.	9487d15d-9116-4ff8-a004-ba0835ea091e	2026-05-31	Warnings	Exact identifier application number: M017
Careland Kinesiology Pain Relieving Tape	CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE	Planet (Anhui) Pharmaceutical Co., Ltd.	35d24cfc-9d34-4fd7-9312-1673b092a3b9	2026-05-31	Warnings	Exact identifier application number: M017
Walgreens Scalp Itch Relief	HYDROCORTISONE	Walgreens	34952272-1f9e-c642-e063-6394a90ae2bd	2026-05-29	Warnings	Exact identifier application number: M017
Aspercreme with Lidocaine No-Mess Applicator	LIDOCAINE HYDROCHLORIDE	Chattem, Inc.	8092cde7-28d0-4755-b5c0-5765934e572f	2026-05-29	Warnings	Exact identifier application number: M017
Belladona and Arnica	MENTHOL	Dannso Corp./d.b.a. Essential Products	fc4e63e4-cebc-49ff-8900-7238261d0fe0	2026-05-28	Warnings	Exact identifier application number: M017
Insect Sting Relief	BENZOCAINE, ALCOHOL	Hubei Fanjian Medical Product Co.,Ltd	f30401c1-961e-44dd-e053-2a95a90a69d6	2026-05-28	Warnings	Exact identifier application number: M017
Menthol plus Camphor Pain Relief	MENTHOL, CAMPHOR	Veridian Healthcare	4a054949-0889-7182-e063-6394a90aff5e	2026-05-28	Warnings	Exact identifier application number: M017
Antibacterial Lidocaine Wound Gel	BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE	CVS Pharmacy	960bfe55-87f6-3e51-e053-2995a90a867d	2026-05-27	Warnings	Exact identifier application number: M017
MyDerm Medical 5 Lidocaine Numbing Roll-On	LIDOCAINE	Inspec Solutions	1d466be1-a780-462f-8dd4-87478da096aa	2026-05-27	Warnings	Exact identifier application number: M017
myDerm Cooling Menthol Pain Relief with 50 Percent More Menthol	MENTHOL	Inspec Solutions LLC.	d427d623-c2fd-7d6b-e053-2995a90abdc3	2026-05-27	Warnings	Exact identifier application number: M017
Caldyphen Clear	PRAMOXINE HYDROCHLORIDE AND ZINC ACETATE	Amerisource Bergen	d8802e56-649e-4494-86ee-7ca8841cc28b	2026-05-27	Warnings	Exact identifier application number: M017
Equate Itch Relief Gel	ITCH RELIEF GEL	Walmart, Inc	7d7bb750-017e-c60e-e053-2991aa0ad671	2026-05-26	Warnings	Exact identifier application number: M017
MyDerm Bite and Sting	BENZOCAINE	Medline Industries	bf45c4dd-5814-4602-b96b-f82a44948763	2026-05-26	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
203105	hydrocortisone 1 % Topical Ointment	PSN	92bcbde3-401a-4301-854e-c352852317d6	3
203105	hydrocortisone 0.01 MG/MG Topical Ointment	SCD	92bcbde3-401a-4301-854e-c352852317d6	3
203105	hydrocortisone 1 % Topical Ointment	SY	92bcbde3-401a-4301-854e-c352852317d6	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
37012-018-02	37012001802	1 TUBE in 1 CARTON (37012-018-02) / 28.4 g in 1 TUBE	1 tube	1989-10-03	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Shopko ® Hydrocortisone	Shopko Stores Operating Co., LLC \| Sun Pharma Canada Inc.	2025-07-15	HUMAN OTC DRUG LABEL	3