Live Better

Product NDC: 51143-059
11-digit product format: 511430059
Labeler code: 51143
Product ID: 51143-059_3994b4c1-3c01-6788-e063-6294a90a33a4
Type: HUMAN OTC DRUG
Nonproprietary name: Hydrocortisone
Dosage form: CREAM
Route: TOPICAL
Labeler: The Great Atlantic & Pacific Tea Company
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 1995-08-23
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	51143-059-02	`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	51143-059-02	`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	51143-059-02	`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	51143-059-02	`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	51143-059-02	`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	51143-059-02	`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	51143-059-02	`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	51143-059-02	`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	51143-059-02	`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	51143-059-02	`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	51143-059-02	`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	51143-059-02	`9bebd1f3094a…`	`5416666fcb17…`

Additional Listing Data#

Finished product: Yes
Brand name base: Live Better
Brand name suffix: Hydrocortisone with Aloe
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
106258	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
044e6ee2-98a6-4802-b33d-78b8551356c4	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
3c386306-c48a-413e-bb69-70cb268496f3	Product name	1	20210727
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
51143-059-02	2024-11-08	C162847	48780-1	9d75b9d0-889f-f424-e053-dadaa90a57ce	Live Better Hydrocortisone with Aloe
51143-059-02	2020-01-31	C162847	48780-1	9d75b9d0-889f-f424-e053-dadaa90a57ce	Live Better Hydrocortisone with Aloe

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
51143-059-02	Live BetterHydrocortisone with Aloe	1 in 1 CARTON	CREAM	1		3
51143-059-02	Live BetterHydrocortisone with Aloe	28.4 g in 1 TUBE	CREAM	28.4		3

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Hydrocortisone	ACTIVE INGREDIENT	WI4X0X7BPJ	LIVE BETTER HYDROCORTISONE WITH ALOE (HYDROCORTISONE) CREAM [THE GREAT ATLANTIC & PACIFIC TEA COMPANY]	1
Hydrocortisone	ACTIVE MOIETY	WI4X0X7BPJ	LIVE BETTER HYDROCORTISONE WITH ALOE (HYDROCORTISONE) CREAM [THE GREAT ATLANTIC & PACIFIC TEA COMPANY]	1
cetostearyl alcohol	INACTIVE INGREDIENT	2DMT128M1S	LIVE BETTER HYDROCORTISONE WITH ALOE (HYDROCORTISONE) CREAM [THE GREAT ATLANTIC & PACIFIC TEA COMPANY]	1
citric acid monohydrate	INACTIVE INGREDIENT	2968PHW8QP	LIVE BETTER HYDROCORTISONE WITH ALOE (HYDROCORTISONE) CREAM [THE GREAT ATLANTIC & PACIFIC TEA COMPANY]	1
glycerin	INACTIVE INGREDIENT	PDC6A3C0OX	LIVE BETTER HYDROCORTISONE WITH ALOE (HYDROCORTISONE) CREAM [THE GREAT ATLANTIC & PACIFIC TEA COMPANY]	1
glyceryl monostearate	INACTIVE INGREDIENT	230OU9XXE4	LIVE BETTER HYDROCORTISONE WITH ALOE (HYDROCORTISONE) CREAM [THE GREAT ATLANTIC & PACIFIC TEA COMPANY]	1
methylparaben	INACTIVE INGREDIENT	A2I8C7HI9T	LIVE BETTER HYDROCORTISONE WITH ALOE (HYDROCORTISONE) CREAM [THE GREAT ATLANTIC & PACIFIC TEA COMPANY]	1
mineral oil	INACTIVE INGREDIENT	T5L8T28FGP	LIVE BETTER HYDROCORTISONE WITH ALOE (HYDROCORTISONE) CREAM [THE GREAT ATLANTIC & PACIFIC TEA COMPANY]	1
paraffin	INACTIVE INGREDIENT	I9O0E3H2ZE	LIVE BETTER HYDROCORTISONE WITH ALOE (HYDROCORTISONE) CREAM [THE GREAT ATLANTIC & PACIFIC TEA COMPANY]	1
propylparaben	INACTIVE INGREDIENT	Z8IX2SC1OH	LIVE BETTER HYDROCORTISONE WITH ALOE (HYDROCORTISONE) CREAM [THE GREAT ATLANTIC & PACIFIC TEA COMPANY]	1
sodium cetostearyl sulfate	INACTIVE INGREDIENT	7ZBS06BH4B	LIVE BETTER HYDROCORTISONE WITH ALOE (HYDROCORTISONE) CREAM [THE GREAT ATLANTIC & PACIFIC TEA COMPANY]	1
sodium lauryl sulfate	INACTIVE INGREDIENT	368GB5141J	LIVE BETTER HYDROCORTISONE WITH ALOE (HYDROCORTISONE) CREAM [THE GREAT ATLANTIC & PACIFIC TEA COMPANY]	1
stearyl alcohol	INACTIVE INGREDIENT	2KR89I4H1Y	LIVE BETTER HYDROCORTISONE WITH ALOE (HYDROCORTISONE) CREAM [THE GREAT ATLANTIC & PACIFIC TEA COMPANY]	1
water	INACTIVE INGREDIENT	059QF0KO0R	LIVE BETTER HYDROCORTISONE WITH ALOE (HYDROCORTISONE) CREAM [THE GREAT ATLANTIC & PACIFIC TEA COMPANY]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51143-059	LIVE BETTER HYDROCORTISONE WITH ALOE (HYDROCORTISONE) CREAM [THE GREAT ATLANTIC & PACIFIC TEA COMPANY]	2	Current NDC, Legacy NDC, 2 package rows	20241109_044e6ee2-98a6-4802-b33d-78b8551356c4.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 31 of 155 · 3,098 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MEDISTIK PROFESSIONAL DUAL ACTION	MENTHOL, METHYL SALICYLATE, EUCALUPTUS	Natureteq Inc.	99c7f08a-ab14-4371-9147-189f75cb6633	2026-02-27	Warnings	Exact identifier application number: M017
Aloe Vera Gel	LIDOCAINE HCL, MENTHOL	Walmart Inc.	309dcf5b-7166-976a-e063-6394a90af952	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M017
ASYSTEM Radical Relief Gel Roll-On	MENTHOL, METHYL SALICYLATE	Cosco International, Inc.	7239733e-5510-4a63-96c3-dd88b4a431a3	2026-02-27	Warnings	Exact identifier application number: M017
Icy Hot Pro Pain Massaging Balm	CAMPHOR AND MENTHOL	Chattem, Inc.	09e2b0cb-5186-4f9c-b256-edaced4ca014	2026-02-27	Warnings	Exact identifier application number: M017
Lidocaine Pain Relief	LIDOCAINE PAIN RELIEF	PAI Holdings, LLC dba PAI Pharma	963978de-8295-47ee-9b06-64c3521aa994	2026-02-26	Warnings	Exact identifier application number: M017
Tommie Copper Cooling Roller Lavender Scent	MENTHOL 4%	Tommie Copper, Inc.	4bbfd4d1-9036-bc20-e063-6394a90a3feb	2026-02-26	Warnings	Exact identifier application number: M017
HQLSEY QUIT SMOKING PATCHES	QUIT SMOKING PATCHES	Hansen Pharmaceutical Investment Co., Limited	4ba317fb-714a-05cb-e063-6394a90a382f	2026-02-25	Warnings	Exact identifier application number: M017
Advanced Pain Relief Cream With 5 % Natural Menthol	MENTHOL	Allure Labs	4bab9c43-86d4-dad2-e063-6394a90ac095	2026-02-25	Warnings	Exact identifier application number: M017
Walgreens Pain Relieving Patch	MENTHOL, CAMPHOR, METHYL SALICYLATE	Walgreen Co.	4223c74a-12fb-51a3-e063-6294a90a0deb	2026-02-25	Warnings	Exact identifier application number: M017
Advanced Pain Relief Roll-On Gel With 5% Natural Menthol	MENTHOL	Allure Labs	4bad597f-acb2-a122-e063-6394a90a9fcf	2026-02-25	Warnings	Exact identifier application number: M017
Maximum Strength 4% Lidocaine Patch Good Neighbor Pharmacy	LIDOCAINE	InterMed Laboratories Private Limited	4bade8a9-43bd-b649-e063-6294a90a81da	2026-02-25	Warnings	Exact identifier application number: M017
dermaFIT Muscle Retention Cream Strength	MENTHOL	EX Healthcare Inc.	4620c41a-2187-00f5-e063-6394a90a613c	2026-02-23	Warnings	Exact identifier application number: M017
dermaFIT Muscle Retention Cream Sculpt	MENTHOL	EX Healthcare Inc.	4620d4ca-42e4-eeae-e063-6394a90a5c84	2026-02-23	Warnings	Exact identifier application number: M017
dermaFIT Muscle Retention Cream Extra Strength	MENTHOL	EX Healthcare Inc.	4620ca7a-afe6-d063-e063-6394a90ab5db	2026-02-23	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE	Sportpharm LLC	9578b39e-3df7-4d75-abd7-f1d5524545e5	2026-02-23	Warnings	Exact identifier application number: M017
0.5% LIDOCAINE BURN RELIEF	LIDOCAINE HYDROCHLORIDE	Nantong Health & Beyond Hygienic Products Inc.	cf723c7b-495d-4bae-942c-561cf28af2d3	2026-02-21	Warnings	Exact identifier application number: M017
Swiftalyn Numbing Cream	MENTHOL 1%	GENUINE INNOVATION LTD	4b2ebff2-2f50-e54b-e063-6294a90aaccb	2026-02-19	Warnings	Exact identifier application number: M017
Equate Cold Therapy Pain Relieving	MENTHOL	Walmart Inc	46a3c9e9-5cd3-4bc4-e063-6394a90a7178	2026-02-19	Warnings	Exact identifier application number: M017
Itch Relief	DIPHENHYDRAMINE HCL, ZINC ACETATE	Meijer, Inc.	e11390ec-99a3-4ff1-a3c8-ca909f4f67b5	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M017
CVS Cold and Hot Pain Relief Dry	LIDOCAINE, MENTHOL	CVS Pharmacy	4b333300-1ae7-a080-e063-6394a90a1372	2026-02-19	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
106258	hydrocortisone 1 % Topical Cream	PSN	044e6ee2-98a6-4802-b33d-78b8551356c4	3
106258	hydrocortisone 10 MG/ML Topical Cream	SCD	044e6ee2-98a6-4802-b33d-78b8551356c4	3
106258	hydrocortisone 1 % (as hydrocortisone acetate 1.2 % ) Topical Cream	SY	044e6ee2-98a6-4802-b33d-78b8551356c4	3
106258	hydrocortisone 1 % Topical Cream	SY	044e6ee2-98a6-4802-b33d-78b8551356c4	3
106258	hydrocortisone 1 GM per 100 GM Topical Cream	SY	044e6ee2-98a6-4802-b33d-78b8551356c4	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
51143-059-02	51143005902	1 TUBE in 1 CARTON (51143-059-02) / 28.4 g in 1 TUBE	1 tube	1995-08-23	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Live Better Hydrocortisone with Aloe	The Great Atlantic & Pacific Tea Company \| Sun Pharma Canada Inc.	2025-07-10	HUMAN OTC DRUG LABEL	3