Banophen

Product NDC: 0904-5354
11-digit product format: 009045354
Labeler code: 0904
Product ID: 0904-5354_9d9d4074-238a-49d0-a5ef-39414da07434
Type: HUMAN OTC DRUG
Nonproprietary name: Diphenhydramine Hydrochloride, Zinc Acetate
Dosage form: CREAM
Route: TOPICAL
Labeler: Major Pharmaceuticals
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2009-06-19
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

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: Banophen
Listing expiration: 2027-12-31

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 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1087026	Internal RxNorm lookup
1092428	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
9758d886-bd58-4eb2-a827-fa8e7fee2b7c	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
0904-5354-31	Banophen	1 in 1 CARTON	CREAM	1		5
0904-5354-31	Banophen	28 g in 1 TUBE	CREAM	28		5

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0904-5354-31	GM - Gram	0904-5354	6a476b0d-917c-4d7b-9b92-2d7e56108466	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
DIPHENHYDRAMINE HYDROCHLORIDE	ACTIVE INGREDIENT	TC2D6JAD40	DIPHENHYDRAMINE (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [PHYSICIANS TOTAL CARE, INC.]	1
DIPHENHYDRAMINE HYDROCHLORIDE	ACTIVE INGREDIENT	TC2D6JAD40	BANOPHEN (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [MAJOR PHARMACEUTICALS]	1
ZINC ACETATE	ACTIVE INGREDIENT	FM5526K07A	DIPHENHYDRAMINE (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [PHYSICIANS TOTAL CARE, INC.]	1
ZINC ACETATE	ACTIVE INGREDIENT	FM5526K07A	BANOPHEN (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [MAJOR PHARMACEUTICALS]	1
DIPHENHYDRAMINE	ACTIVE MOIETY	8GTS82S83M	DIPHENHYDRAMINE (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [PHYSICIANS TOTAL CARE, INC.]	1
DIPHENHYDRAMINE	ACTIVE MOIETY	8GTS82S83M	BANOPHEN (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [MAJOR PHARMACEUTICALS]	1
ZINC	ACTIVE MOIETY	J41CSQ7QDS	DIPHENHYDRAMINE (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [PHYSICIANS TOTAL CARE, INC.]	1
ZINC	ACTIVE MOIETY	J41CSQ7QDS	BANOPHEN (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [MAJOR PHARMACEUTICALS]	1
CETYL ALCOHOL	INACTIVE INGREDIENT	936JST6JCN	DIPHENHYDRAMINE (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [PHYSICIANS TOTAL CARE, INC.]	1
DIAZOLIDINYL UREA	INACTIVE INGREDIENT	H5RIZ3MPW4	DIPHENHYDRAMINE (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [PHYSICIANS TOTAL CARE, INC.]	1
METHYLPARABEN	INACTIVE INGREDIENT	A2I8C7HI9T	DIPHENHYDRAMINE (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [PHYSICIANS TOTAL CARE, INC.]	1
PEG-2 STEARATE	INACTIVE INGREDIENT	94YQ11Y95F	DIPHENHYDRAMINE (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [PHYSICIANS TOTAL CARE, INC.]	1
PEG-20 STEARATE	INACTIVE INGREDIENT	NBX892EA57	DIPHENHYDRAMINE (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [PHYSICIANS TOTAL CARE, INC.]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	DIPHENHYDRAMINE (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [PHYSICIANS TOTAL CARE, INC.]	1
PROPYLPARABEN	INACTIVE INGREDIENT	Z8IX2SC1OH	DIPHENHYDRAMINE (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [PHYSICIANS TOTAL CARE, INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	DIPHENHYDRAMINE (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [PHYSICIANS TOTAL CARE, INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0904-5354	BANOPHEN (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE) CREAM [MAJOR PHARMACEUTICALS]	4	Current NDC, Legacy NDC, 2 package rows	20240926_9758d886-bd58-4eb2-a827-fa8e7fee2b7c.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 14 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Roll Pain Away	CAPSAICIN	PROXIMITY CAPITAL PARTNERS LLC DBA ASUTRA	547e647b-0205-221c-e063-6294a90a757c	2026-06-17	Warnings	Exact identifier application number: M017
Roll Pain Away Lemongrass	CAPSAICIN	PROXIMITY CAPITAL PARTNERS LLC DBA ASUTRA	547ef5c0-bc31-d83e-e063-6394a90abfa6	2026-06-17	Warnings	Exact identifier application number: M017
Roll Pain Away Lavender	CAPSAICIN	PROXIMITY CAPITAL PARTNERS LLC DBA ASUTRA	547ef2d9-f5c7-9de1-e063-6394a90a218b	2026-06-17	Warnings	Exact identifier application number: M017
Velloryn EXTRA STRENGTH NEUROPATHY	VELLORYN EXTRA STRENGTH NEUROPATHY	GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd	547f755f-c65c-37ef-e063-6394a90aa220	2026-06-17	Warnings	Exact identifier application number: M017
Neoteric Diabetic Skin Care 4 oz.	DIMETHICONE	RNA PHARMA LLC	536f4e79-201b-7100-e063-6394a90a4f82	2026-06-16	Warnings	Exact identifier application number: M017
Medi First Extra Strength Itch Relief	DIPHENHYDRAMINE, ZINC ACETATE	Unifirst First Aid Corporation	54614e5b-8c72-d308-e063-6294a90a405d	2026-06-16	Warnings	Exact identifier application number: M017
Blue Ice Analgesic	MENTHOL	Delon Laboratories (1990) Ltd	184ed488-6e62-40c6-bb71-1d523280fd6b	2026-06-16	Warnings	Exact identifier application number: M017
Medi-First Hydrocortisone 1 % Anti-Itch Cream	HYDROCORTISONE	Unifirst First Aid Corporation	49f04e5d-746d-cbe9-e063-6294a90a7e88	2026-06-16	Warnings	Exact identifier application number: M017
Lidozall Pro	LIDOCAINE HYDROCHLORIDE	V2 Pharma LLC	ecc26ba7-4ff6-43e6-bfb9-91a9cbb509ff	2026-06-16	Warnings	Exact identifier application number: M017
Tiger Balm Pain Relieving Cool	CAMPHOR (SYNTHETIC) AND MENTHOL, UNSPECIFIED FORM	Haw Par Healthcare Ltd.	41590ba1-32bb-4352-97ba-d6a3cc9d0546	2026-06-15	Warnings	Exact identifier application number: M017
HIGH POTENCY PAIN RELIEF	CAPSAICIN	Xiamen Weisiqi Technology Co., Ltd.	543949a4-86ed-3734-e063-6394a90a24f2	2026-06-14	Warnings	Exact identifier application number: M017
Natucure HEMORRHOID	LIDOCAINE 4% PHENYLEPHRINE HCL 0.25% HEMORRHOID	Jiangxi Yudexi Pharmaceutical Co., LTD	49e402ed-d314-e896-e063-6294a90a826b	2026-06-14	Warnings	Exact identifier application number: M017
Nieapf NUMBING	LIDOCAINE 4% NUMBING	Jiangxi Yudexi Pharmaceutical Co., LTD	49e7534f-bccf-4ef4-e063-6294a90aeb7f	2026-06-14	Warnings	Exact identifier application number: M017
HEALMUSZ NUMBING	HEALMUSZ NUMBING	Jiangxi Yudexi Pharmaceutical Co., LTD	49976ff7-49a4-e4ed-e063-6294a90a3f78	2026-06-14	Warnings	Exact identifier application number: M017
HEALMUSZ HEMORRHOID FISSURE	LIDOCAINE 4% PHENYLEPHRINE HCL 0.25% HEMORRHOID FISSURE	Jiangxi Yudexi Pharmaceutical Co., LTD	4a342ac0-6a8d-3408-e063-6394a90a9a10	2026-06-14	Warnings	Exact identifier application number: M017
BOTASUN QUIT SMOKING Nicotine	NICOTINE18% MENTHOL 0.3% QUIT SMOKING NICOTINE	Jiangxi Yudexi Pharmaceutical Co., LTD	4fa00db9-def5-dcfa-e063-6394a90ac8c2	2026-06-14	Warnings	Exact identifier application number: M017
HEALMUSZ NUMBING	MENTHOL 5% NUMBING	Jiangxi Yudexi Pharmaceutical Co., LTD	4cbb7df5-5771-ce4b-e063-6294a90aab80	2026-06-14	Warnings	Exact identifier application number: M017
HEALMUSZ ECZEMA	HYDROCORTISONE 1% ECZEMA	Jiangxi Yudexi Pharmaceutical Co., LTD	511e54e0-2abe-fb76-e063-6294a90ada68	2026-06-14	Warnings	Exact identifier application number: M017
Hydrocortisone 1% Anti-ItchCream	HYDROCORTISONE	Acme United Corporation	5425fc2b-4f25-3e64-e063-6394a90aff49	2026-06-13	Warnings	Exact identifier application number: M017
Icy Hot Pain Relieving Balm	MENTHOL AND METHYL SALICYLATE	Chattem, Inc.	40c8c02f-fa5f-4e80-81a0-48271fa6f94b	2026-06-12	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
1092428	Banophen Cream 2 % / 0.1 % Topical Cream	PSN	9758d886-bd58-4eb2-a827-fa8e7fee2b7c	5
1087026	diphenhydrAMINE HCl 2 % / zinc acetate 0.1 % Topical Cream	PSN	9758d886-bd58-4eb2-a827-fa8e7fee2b7c	5
1092428	diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical Cream [Banophen Cream]	SBD	9758d886-bd58-4eb2-a827-fa8e7fee2b7c	5
1087026	diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical Cream	SCD	9758d886-bd58-4eb2-a827-fa8e7fee2b7c	5
1092428	Banophen Cream (diphenhydramine hydrochloride 2 % / zinc acetate 0.1 % ) Topical Cream	SY	9758d886-bd58-4eb2-a827-fa8e7fee2b7c	5
1087026	diphenhydramine hydrochloride 2 % / zinc acetate 0.1 % Topical Cream	SY	9758d886-bd58-4eb2-a827-fa8e7fee2b7c	5
1087026	diphenhydrAMINE HCl 2 % / zinc acetate 0.1 % Topical Cream	PSN	82e6a91c-fb8b-42b5-8b01-3db180b9d7fc	1
1087026	diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical Cream	SCD	82e6a91c-fb8b-42b5-8b01-3db180b9d7fc	1
1087026	diphenhydramine hydrochloride 2 % / zinc acetate 0.1 % Topical Cream	SY	82e6a91c-fb8b-42b5-8b01-3db180b9d7fc	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0904-5354-31	00904535431	1 TUBE in 1 CARTON (0904-5354-31) / 28 g in 1 TUBE	1 tube	2009-06-19	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Major Pharmaceuticals Banophen™ Drug Facts	Major Pharmaceuticals	2026-02-13	HUMAN OTC DRUG LABEL	5
Diphenhydramine - Physicians Total Care, Inc.	Physicians Total Care, Inc.	2012-06-05	HUMAN OTC DRUG LABEL	1