berkley and jensen anti itch

Product NDC: 68391-100
11-digit product format: 683910100
Labeler code: 68391
Product ID: 68391-100_1957807a-362b-41b6-9243-2d1ece9f7c95
Type: HUMAN OTC DRUG
Nonproprietary name: Hydrocortisone
Dosage form: CREAM
Route: TOPICAL
Labeler: BJWC
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2014-12-09
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 · 2 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2020-06-10 20:45 UTC · source 2020-06-10	excluded product	product	68391-100		I	Inactivated by FDA		excluded / ndc_excluded.zip	`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	68391-100	68391-100-16	I	Inactivated by FDA		excluded / ndc_excluded.zip	`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: berkley and jensen anti itch
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
5cc6e4f6-c62d-4923-9726-9dbc569a3f49	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
68391-100-16	2020-08-05	C162847	48780-1	9d75b9d0-ad2f-f424-e053-dadaa90a57ce	BJWC Anti-Itch Cream Drug Facts
68391-100-16	2020-01-31	C162847	48780-1	9d75b9d0-ad2f-f424-e053-dadaa90a57ce	BJWC Anti-Itch Cream Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68391-100-16	berkley and jensen anti itch	56 g in 1 TUBE	CREAM	56		4
68391-100-16	berkley and jensen anti itch	2 in 1 CARTON	CREAM	2		4

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
HYDROCORTISONE	ACTIVE INGREDIENT	WI4X0X7BPJ	BERKLEY AND JENSEN ANTI ITCH (HYDROCORTISONE) CREAM [BJWC]	1
HYDROCORTISONE	ACTIVE MOIETY	WI4X0X7BPJ	BERKLEY AND JENSEN ANTI ITCH (HYDROCORTISONE) CREAM [BJWC]	1
ALOE VERA LEAF	INACTIVE INGREDIENT	ZY81Z83H0X	BERKLEY AND JENSEN ANTI ITCH (HYDROCORTISONE) CREAM [BJWC]	1
CETOSTEARYL ALCOHOL	INACTIVE INGREDIENT	2DMT128M1S	BERKLEY AND JENSEN ANTI ITCH (HYDROCORTISONE) CREAM [BJWC]	1
CETYL PALMITATE	INACTIVE INGREDIENT	5ZA2S6B08X	BERKLEY AND JENSEN ANTI ITCH (HYDROCORTISONE) CREAM [BJWC]	1
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	BERKLEY AND JENSEN ANTI ITCH (HYDROCORTISONE) CREAM [BJWC]	1
ISOPROPYL MYRISTATE	INACTIVE INGREDIENT	0RE8K4LNJS	BERKLEY AND JENSEN ANTI ITCH (HYDROCORTISONE) CREAM [BJWC]	1
METHYLPARABEN	INACTIVE INGREDIENT	A2I8C7HI9T	BERKLEY AND JENSEN ANTI ITCH (HYDROCORTISONE) CREAM [BJWC]	1
POLYOXYL 20 CETOSTEARYL ETHER	INACTIVE INGREDIENT	YRC528SWUY	BERKLEY AND JENSEN ANTI ITCH (HYDROCORTISONE) CREAM [BJWC]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	BERKLEY AND JENSEN ANTI ITCH (HYDROCORTISONE) CREAM [BJWC]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68391-100	BERKLEY AND JENSEN ANTI ITCH (HYDROCORTISONE) CREAM [BJWC]	4	Current NDC, Legacy NDC, 2 package rows	20241023_5cc6e4f6-c62d-4923-9726-9dbc569a3f49.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 139 of 151 · 3,020 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
XRay Pain Relief	MENTHOL, (PLUS)-, CAMPHOR, (-)-, AND METHYL SALICYLATE	Genomma Lab USA	5244ddee-fd9e-4df3-8fb3-b16aa321a316	2023-12-27	Warnings	Exact identifier application number: M017
Camphor Spirit	CAMPHOR 10%	Pharma Nobis, LLC	e42fbe63-b01c-4f85-e053-2a95a90a5143	2023-12-26	Warnings	Exact identifier application number: M017
Equate Calaspray	PRAMOXINE HCL 1%, ZINC ACETATE 0.1%	Walmart Inc	027ed5ab-05ec-569f-e063-6394a90abbc3	2023-12-26	Warnings	Exact identifier application number: M017
EXTERNAL ANALGESIC	CAMPHOR, CAPSICUM, MENTHOL	Hmong 21	3b6155a5-51aa-2780-e054-00144ff8d46c	2023-12-26	Warnings	Exact identifier application number: M017
LEADER Camphor Spirit	CAMPHOR (NATURAL)	Cardinal Health, 110 dba Leader	7d3b0b28-5190-0622-e053-2991aa0af561	2023-12-22	Warnings	Exact identifier application number: M017
Antiseptic Instant Pain Relief	CAMPHOR 10.8% AND PHENOL 4.7%	Pharma Nobis, LLC	e42f484d-a642-3489-e053-2a95a90a4254	2023-12-22	Warnings	Exact identifier application number: M017
Itch Relief Gel	ITCH RELIEF GEL	Pharma Nobis, LLC	e42f484d-a641-3489-e053-2a95a90a4254	2023-12-22	Warnings	Exact identifier application number: M017
Witch Hazel	WITCH HAZEL	Pharma Nobis, LLC	e42f484d-a644-3489-e053-2a95a90a4254	2023-12-22	Warnings	Exact identifier application number: M017
Dermoplast Pain relieving	BENZOCAINE, MENTHOL	Advantice Health	dad00c95-4e11-3eec-e053-2a95a90a7a18	2023-12-21	Warnings	Exact identifier application number: M017
equate Maximum Strength Pain Relieving 4% Lidocaine with Lavender Essential Oil Topical analgesic	LIDOCAINE HYDROCHLORIDE	Wal-Mart Stores, Inc.	bf954949-a7b7-44ba-8565-f1d5c0a6c0d1	2023-12-21	Warnings	Exact identifier application number: M017
Bactine Max Bandage	LIDOCAINE	WellSpring Pharmaceutical Corporation	465dc46e-6435-4569-9516-f648d0fe0f09	2023-12-21	Warnings	Exact identifier application number: M017
Valtrum IMMEDIATE ACTION TOPICAL ANALGESIC	CAMPHOR, MENTHOL, METHYL SALICYLATE	LABORATORIOS QUANTIUM LLC	c4efa317-8dd1-49e1-b7ca-9df2147edd3e	2023-12-21	Warnings	Exact identifier application number: M017
DDM Camphor Spirit	CAMPHOR 10%	Discount Drug Mart	5d56cbe6-4e48-79eb-e053-2a91aa0a74d3	2023-12-20	Warnings	Exact identifier application number: M017
Quality Choice Camphor Spirit	CAMPHOR 10%	Chain Drug Market Association	8d352a67-2024-43d0-b525-038d398949e6	2023-12-20	Warnings	Exact identifier application number: M017
Instant Antiseptic Pain Relief	CAMPHOR 10.8% AND PHENOL 4.7%	Chain Drug Market Association	2cd60df3-bfde-4747-ba4f-7121612f2e63	2023-12-20	Warnings	Exact identifier application number: M017
Poison Ivy Wash	PRAMOXINE HCL	Chain Drug Market Association	873a546b-90ae-50cb-e053-2a91aa0adbfb	2023-12-20	Warnings	Exact identifier application number: M017
Premier Value Instant Antiseptic Pain Relief	CAMPHOR 10.8% AND PHENOL 4.7%	Pharmacy Value Alliance LLC	9d63f8ed-fc50-0d84-e053-2a95a90a6e92	2023-12-20	Warnings	Exact identifier application number: M017
Ear Drops	CARBAMIDE PEROXIDE 6.5%	CVS Pharmacy	8a872991-01af-5fd0-e053-2995a90ac7f4	2023-12-20	Warnings	Exact identifier application number: M017
CVS Cold and Hot Roll-On	COOL AND HEAT PAIN RELIEF	CVS Pharmacy	b8cc578a-be6d-90c0-e053-2995a90a7742	2023-12-20	Warnings	Exact identifier application number: M017
Sunmark Camphor Spirit	CAMPHOR 10%	Strategic Sourcing Services LLC	667b3a9f-4a5c-4ef0-adbd-cce9a5f94faa	2023-12-19	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	5cc6e4f6-c62d-4923-9726-9dbc569a3f49	4
106258	hydrocortisone 10 MG/ML Topical Cream	SCD	5cc6e4f6-c62d-4923-9726-9dbc569a3f49	4
106258	hydrocortisone 1 % (as hydrocortisone acetate 1.2 % ) Topical Cream	SY	5cc6e4f6-c62d-4923-9726-9dbc569a3f49	4
106258	hydrocortisone 1 % Topical Cream	SY	5cc6e4f6-c62d-4923-9726-9dbc569a3f49	4
106258	hydrocortisone 1 GM per 100 GM Topical Cream	SY	5cc6e4f6-c62d-4923-9726-9dbc569a3f49	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
68391-100-16	68391010016	2 TUBE in 1 CARTON (68391-100-16) / 56 g in 1 TUBE	2 tube	2014-12-09	0000-00-00	No	No	Current