itch relief

Product NDC: 37808-622
11-digit product format: 378080622
Labeler code: 37808
Product ID: 37808-622_73bec294-055a-4342-9cdf-00cd83e1d0ad
Type: HUMAN OTC DRUG
Nonproprietary name: Diphenhydramine Hydrochloride, Zinc Acetate
Dosage form: CREAM
Route: TOPICAL
Labeler: H E B
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2010-09-15
Substance: DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE
Active strength: 2; .1 g/100g; g/100g
Pharmacologic classes: Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag: No
Listing certified through: 2027-12-31
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
2019-12-08 06:16 UTC · source 2019-12-05	excluded product	product	37808-622		E	Excluded after deficient or non-compliant submission was not corrected		excluded / ndc_excluded.zip	`110d247fa046…`	`a55b01930146…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded package	package	37808-622	37808-622-64	E	Excluded after deficient or non-compliant submission was not corrected		excluded / ndc_excluded.zip	`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: itch relief
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
DIPHENHYDRAMINE HYDROCHLORIDE	2 g/100g
ZINC ACETATE	.1 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
TC2D6JAD40	Internal UNII lookup
FM5526K07A	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1087026	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
34c7bcd3-203f-4630-894d-3739a1576c8d	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
f47a510b-6679-4664-b2d6-47b5c4afe7cc	Product name	4	20260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61c	Product name	2	20250515
0e2e0f88-b076-afe1-4bdd-32bca4375bec	Product name	3	20250127
0306390c-dd77-4363-afe0-63c58088b2a1	Product name	1	20220120
503ea967-4b9c-48cf-9e87-c7975295849d	Product name	2	20220120
190f2a5b-bbc8-65c7-fcb0-97891307b917	Product name	1	20140508
3e48c9c4-918d-5d23-2f0b-d2398b06be54	Product name	1	20140508
865c72dd-0d94-daac-f728-ddd4ded2a79e	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
37808-622-64	itch relief	1 in 1 CARTON	CREAM	1		3
37808-622-64	itch relief	28 g in 1 TUBE	CREAM	28		3

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
DIPHENHYDRAMINE HYDROCHLORIDE	ACTIVE INGREDIENT	TC2D6JAD40	ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [H E B]	1
ZINC ACETATE	ACTIVE INGREDIENT	FM5526K07A	ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [H E B]	1
DIPHENHYDRAMINE	ACTIVE MOIETY	8GTS82S83M	ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [H E B]	1
ZINC	ACTIVE MOIETY	J41CSQ7QDS	ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [H E B]	1
CETYL ALCOHOL	INACTIVE INGREDIENT	936JST6JCN	ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [H E B]	1
DIAZOLIDINYL UREA	INACTIVE INGREDIENT	H5RIZ3MPW4	ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [H E B]	1
METHYLPARABEN	INACTIVE INGREDIENT	A2I8C7HI9T	ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [H E B]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [H E B]	1
PROPYLPARABEN	INACTIVE INGREDIENT	Z8IX2SC1OH	ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [H E B]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [H E B]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
37808-622	ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [H E B]	3	Current NDC, Legacy NDC, 2 package rows	20241015_34c7bcd3-203f-4630-894d-3739a1576c8d.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 68 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
PAINGEL UNGUENTO	CAMPHOR, MENTHOL	NACOR BUSINESS GROUP LLC	42fab525-b0a5-97fb-e063-6394a90aec6c	2025-11-06	Warnings	Exact identifier application number: M017
PAINGEL ROLL-ON	MENTHOL	NACOR BUSINESS GROUP LLC	42fb0bdf-8bbd-bbe3-e063-6294a90a656c	2025-11-06	Warnings	Exact identifier application number: M017
Coolexa	CAMPHOR, MENTHOL, METHYL SALICYLATE	Rising Pharma Holdings, Inc.	38839f29-d4ce-4684-a3c7-0bb4bf1ad594	2025-11-06	Warnings	Exact identifier application number: M017
ItchZap	DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE	Rising Pharma Holdings, Inc.	245d0afb-19a8-4cfb-968b-d892b18d5f2c	2025-11-06	Warnings	Exact identifier application number: M017
Pain Relief Gel-Roll On	LIDOCAINE AND MENTHOL	Bullet point LLC	42c70681-494b-47c9-e063-6394a90a80be	2025-11-04	Warnings	Exact identifier application number: M017
China-Gel Topical Pain Reliever	MENTHOL AND CAMOHOR (SYNTHETIC)	China-Gel, LLC	ba6c7e97-d740-484b-8711-55fa7ab15784	2025-11-04	Warnings	Exact identifier application number: M017
China-Gel	MENTHOL AND CAMOHOR (SYNTHETIC)	China-Gel, Inc.	d7c5cb17-f7a2-7f57-e053-2995a90a40f7	2025-11-04	Warnings	Exact identifier application number: M017
Aulief Topical Pain Reliever	MENTHOL AND CAMOHOR	China-Gel, LLC	8647dcc3-1dbc-1093-e053-2991aa0a1ab9	2025-11-04	Warnings	Exact identifier application number: M017
China-Gel Topical Pain Reliever	MENTHOL AND CAMOHOR (SYNTHETIC)	China-Gel, LLC	254abae9-ef1b-5a90-e054-00144ff88e88	2025-11-04	Warnings	Exact identifier application number: M017
Pain Relief Gel-Tube	MENTHOL	Bullet point LLC	42c93789-9758-54b7-e063-6394a90ac398	2025-11-04	Warnings	Exact identifier application number: M017
Tattoo care	TATTOO CARE CREAM	Perfso (HK) Co., Limited	42d0f56f-9cb1-8e19-e063-6394a90aa3e0	2025-11-04	Warnings	Exact identifier application number: M017
CORE RELIEF	CAMPHOR, MENTHOL	Copper Joint, LLC	42d17270-f58d-9d69-e063-6294a90a4078	2025-11-04	Warnings	Exact identifier application number: M017
Lidocaine and Menthol	LIDOCAINE AND MENTHOL	Marcella Health	d25f25ee-79f8-49e7-9715-0aae305b73e5	2025-11-03	Warnings	Exact identifier application number: M017
Calamine Plus Pramoxine HCl	CALAMINE PLUS NO TOUCH SPRAY	Premier Brands of America Inc.	36481d67-2346-470b-e063-6294a90aae99	2025-11-03	Warnings	Exact identifier application number: M017
Lidocaine Numbing Cream	LIDOCAINE 5%	YYBA Corp	1319ee69-8b3f-5815-e063-6294a90a5ad5	2025-11-03	Warnings	Exact identifier application number: M017
Goodsense Extra Strength Cold and Hot Medicated	MENTHOL	Geiss, Destin and Dunn, Inc.	7585d111-775f-4fb6-a485-28cd99d88852	2025-10-31	Warnings	Exact identifier application number: M017
Topcare Cold and Hot Medicated	MENTHOL	Topco Associates LLC	8739aedd-165c-5ae0-e053-2a91aa0afcd0	2025-10-31	Warnings	Exact identifier application number: M017
CVS Medicated Heat 1 ct	CAPSAICIN	CVS Pharmacy, Inc.	d41dce5b-e698-4930-8869-040b2a973f25	2025-10-31	Warnings	Exact identifier application number: M017
Coralite Medicated Heat	CAPSAICIN	United Exchange Corp.	a0b89c7e-80bc-43c4-840c-5fd567f60b21	2025-10-31	Warnings	Exact identifier application number: M017
Dragon with Arnical Pain Relief	MENTHOL	Genomma Lab USA Inc.	b4cbb7b6-cb71-9721-e053-2995a90a2b2c	2025-10-31	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
TC2D6JAD40	DIPHENHYDRAMINE HYDROCHLORIDE	147-24-0	DIPHENHYDRAMINE HYDROCHLORIDE
FM5526K07A	ZINC ACETATE	5970-45-6	ZINC ACETATE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1087026	diphenhydrAMINE HCl 2 % / zinc acetate 0.1 % Topical Cream	PSN	34c7bcd3-203f-4630-894d-3739a1576c8d	3
1087026	diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical Cream	SCD	34c7bcd3-203f-4630-894d-3739a1576c8d	3
1087026	diphenhydramine hydrochloride 2 % / zinc acetate 0.1 % Topical Cream	SY	34c7bcd3-203f-4630-894d-3739a1576c8d	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
37808-622-64	37808062264	1 TUBE in 1 CARTON (37808-622-64) / 28 g in 1 TUBE	1 tube	2010-09-15	0000-00-00	No	No	Current