Benadryl

Product NDC: 50580-226
11-digit product format: 505800226
Labeler code: 50580
Product ID: 50580-226_57a6b529-75db-f06e-e063-6294a90a7dd3
Type: HUMAN OTC DRUG
Nonproprietary name: Diphenhydramine Hydrochloride
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Kenvue Brands LLC
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2008-09-01
Substance: DIPHENHYDRAMINE HYDROCHLORIDE
Active strength: 25 mg/1
Pharmacologic classes: 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: Benadryl
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
DIPHENHYDRAMINE HYDROCHLORIDE	25 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

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

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1049630	Internal RxNorm lookup
1049632	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
702f9786-7ce9-43e4-921d-e1db09612127	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
0e2e0f88-b076-afe1-4bdd-32bca4375bec	Product name	3	20250127
3e48c9c4-918d-5d23-2f0b-d2398b06be54	Product name	1	20140508
865c72dd-0d94-daac-f728-ddd4ded2a79e	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
50580-226-50	2024-02-06	Benadryl ®
50580-226-50	2024-02-06	Benadryl ®
50580-226-50	2024-02-06	Benadryl ®
50580-226-51	2024-02-06	Benadryl ®
50580-226-51	2024-02-06	Benadryl ®
50580-226-51	2024-02-06	Benadryl ®
50580-226-52	2024-02-06	Benadryl ®
50580-226-52	2024-02-06	Benadryl ®
50580-226-52	2024-02-06	Benadryl ®
50580-226-53	2024-02-06	Benadryl ®
50580-226-53	2024-02-06	Benadryl ®
50580-226-53	2024-02-06	Benadryl ®
50580-226-54	2024-02-06	Benadryl ®
50580-226-54	2024-02-06	Benadryl ®
50580-226-54	2024-02-06	Benadryl ®
50580-226-56	2024-02-06	Benadryl ®
50580-226-56	2024-02-06	Benadryl ®
50580-226-56	2024-02-06	Benadryl ®
50580-226-62	2024-02-06	Benadryl ®
50580-226-62	2024-02-06	Benadryl ®
50580-226-62	2024-02-06	Benadryl ®
50580-226-50	2024-01-30	Benadryl ®
50580-226-50	2024-01-30	Benadryl ®
50580-226-50	2024-01-30	Benadryl ®
50580-226-51	2024-01-30	Benadryl ®
50580-226-51	2024-01-30	Benadryl ®
50580-226-51	2024-01-30	Benadryl ®
50580-226-52	2024-01-30	Benadryl ®
50580-226-52	2024-01-30	Benadryl ®
50580-226-52	2024-01-30	Benadryl ®
50580-226-53	2024-01-30	Benadryl ®
50580-226-53	2024-01-30	Benadryl ®
50580-226-53	2024-01-30	Benadryl ®
50580-226-54	2024-01-30	Benadryl ®
50580-226-54	2024-01-30	Benadryl ®
50580-226-54	2024-01-30	Benadryl ®
50580-226-56	2024-01-30	Benadryl ®
50580-226-56	2024-01-30	Benadryl ®
50580-226-56	2024-01-30	Benadryl ®
50580-226-62	2024-01-30	Benadryl ®
50580-226-62	2024-01-30	Benadryl ®
50580-226-62	2024-01-30	Benadryl ®

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
50580-226-12	Benadryl	1 in 1 CARTON	TABLET, FILM COATED	1	31
50580-226-12	Benadryl	12 in 1 BLISTER PACK	TABLET, FILM COATED	12	31
50580-226-20	Benadryl	1 in 1 CARTON	TABLET, FILM COATED	1	31
50580-226-20	Benadryl	2 in 1 CARTON	TABLET, FILM COATED	2	31
50580-226-33	Benadryl	3 in 1 CARTON	TABLET, FILM COATED	3	31
50580-226-33	Benadryl	1 in 1 CARTON	TABLET, FILM COATED	1	31
50580-226-50	Benadryl	100 in 1 BOTTLE	TABLET, FILM COATED	100	31
50580-226-50	Benadryl	1 in 1 CARTON	TABLET, FILM COATED	1	31
50580-226-51	Benadryl	12 in 1 BLISTER PACK	TABLET, FILM COATED	12	31
50580-226-51	Benadryl	2 in 1 CARTON	TABLET, FILM COATED	2	31
50580-226-52	Benadryl	4 in 1 CARTON	TABLET, FILM COATED	4	31
50580-226-52	Benadryl	12 in 1 BLISTER PACK	TABLET, FILM COATED	12	31
50580-226-53	Benadryl	2 in 1 POUCH	TABLET, FILM COATED	2	31
50580-226-54	Benadryl	60 in 1 CARTON	TABLET, FILM COATED	60	31
50580-226-54	Benadryl	2 in 1 POUCH	TABLET, FILM COATED	2	31
50580-226-56	Benadryl	3 in 1 PACKAGE	TABLET, FILM COATED	3	31
50580-226-56	Benadryl	4 in 1 CARTON	TABLET, FILM COATED	4	31
50580-226-62	Benadryl	2 in 1 POUCH	TABLET, FILM COATED	2	31
50580-226-62	Benadryl	4 in 1 CARTON	TABLET, FILM COATED	4	31
50580-226-70	Benadryl	48 in 1 BOTTLE	TABLET, FILM COATED	48	31
50580-226-70	Benadryl	1 in 1 CARTON	TABLET, FILM COATED	1	31

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
50580-226-10	EA - Each	50580-226	0e538188-3b26-4cf7-a5d2-7653a4c5807f	1	2012-07-24
50580-226-48	EA - Each	50580-226	30dcc89c-a992-45e8-84cd-964543091fb3	1	2012-07-24
50580-226-50	EA - Each	50580-226	0c74e638-fdc6-4e03-aa02-8f64c6b47a2c	1	2017-12-14
50580-226-51	EA - Each	50580-226	4b1c6774-52e1-41f4-bb46-9e3415756200	1	2013-04-01
50580-226-52	EA - Each	50580-226	05a4b0af-3905-4b1c-88a4-3fb4f226675b	1	2015-10-02
50580-226-54	EA - Each	50580-226	e04fc601-d017-4bc6-94ae-ecd6715d9b2f	1	2022-02-07
50580-226-62	EA - Each	50580-226	f56d0e68-9dd8-4cf9-b5cd-ac5e7c49552b	1	2019-08-06

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Diphenhydramine Hydrochloride	ACTIVE INGREDIENT	TC2D6JAD40	BENADRYL (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [MCNEIL CONSUMER HEALTHCARE DIV MCNEIL-PPC, INC]	7
Diphenhydramine	ACTIVE MOIETY	8GTS82S83M	BENADRYL (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [MCNEIL CONSUMER HEALTHCARE DIV MCNEIL-PPC, INC]	7
Aluminum Oxide	INACTIVE INGREDIENT	LMI26O6933	BENADRYL (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [MCNEIL CONSUMER HEALTHCARE DIV MCNEIL-PPC, INC]	7
Calcium Phosphate, Dibasic, Dihydrate	INACTIVE INGREDIENT	O7TSZ97GEP	BENADRYL (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [MCNEIL CONSUMER HEALTHCARE DIV MCNEIL-PPC, INC]	7
Carnauba Wax	INACTIVE INGREDIENT	R12CBM0EIZ	BENADRYL (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [MCNEIL CONSUMER HEALTHCARE DIV MCNEIL-PPC, INC]	7
Cellulose, Microcrystalline	INACTIVE INGREDIENT	OP1R32D61U	BENADRYL (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [MCNEIL CONSUMER HEALTHCARE DIV MCNEIL-PPC, INC]	7
Croscarmellose Sodium	INACTIVE INGREDIENT	M28OL1HH48	BENADRYL (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [MCNEIL CONSUMER HEALTHCARE DIV MCNEIL-PPC, INC]	7
Crospovidone	INACTIVE INGREDIENT	68401960MK	BENADRYL (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [MCNEIL CONSUMER HEALTHCARE DIV MCNEIL-PPC, INC]	7
D&C Red no. 27	INACTIVE INGREDIENT	2LRS185U6K	BENADRYL (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [MCNEIL CONSUMER HEALTHCARE DIV MCNEIL-PPC, INC]	7
Hypromelloses	INACTIVE INGREDIENT	3NXW29V3WO	BENADRYL (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [MCNEIL CONSUMER HEALTHCARE DIV MCNEIL-PPC, INC]	7
Magnesium Stearate	INACTIVE INGREDIENT	70097M6I30	BENADRYL (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [MCNEIL CONSUMER HEALTHCARE DIV MCNEIL-PPC, INC]	7
Polyethylene Glycols	INACTIVE INGREDIENT	3WJQ0SDW1A	BENADRYL (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [MCNEIL CONSUMER HEALTHCARE DIV MCNEIL-PPC, INC]	7
Polysorbate 80	INACTIVE INGREDIENT	6OZP39ZG8H	BENADRYL (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [MCNEIL CONSUMER HEALTHCARE DIV MCNEIL-PPC, INC]	7
Stearic Acid	INACTIVE INGREDIENT	4ELV7Z65AP	BENADRYL (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [MCNEIL CONSUMER HEALTHCARE DIV MCNEIL-PPC, INC]	7
Titanium Dioxide	INACTIVE INGREDIENT	15FIX9V2JP	BENADRYL (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [MCNEIL CONSUMER HEALTHCARE DIV MCNEIL-PPC, INC]	7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50580-226	BENADRYL (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [KENVUE BRANDS LLC]	28	Current NDC, Legacy NDC, 21 package rows	20250426_702f9786-7ce9-43e4-921d-e1db09612127.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 29 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Allergy Relief	DIPHENHYDRAMINE HCL	L.N.K. International, Inc.	db264d2f-bf81-4da2-8595-2bfa1e4ba2f1	2026-05-18	Warnings	Exact identifier application number: M012
equate nighttime cold and flu	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE	Wal-Mart Stores Inc	b8fc9b0e-8ab7-46e6-9fd9-18f8d4a14b5c	2026-05-15	Warnings	Exact identifier application number: M012
good neighbor pharmacy cold and cough	BROMPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL	Amerisource Bergen	da91e6b6-32ff-44fd-afce-33ea9549554b	2026-05-15	Warnings	Exact identifier application number: M012
Antihistamine	DIPHENHYDRAMINE HCL	Gendose Pharmaceuticals, LLC	847cdee8-410f-4ff3-9245-976ed6f4c776	2026-05-15	Warnings	Exact identifier application number: M012
Antihistamine	DIPHENHYDRAMINE HCL	Gendose Pharmaceuticals, LLC	d3b2f300-d919-44cd-ab71-b74b5bdfd977	2026-05-15	Warnings	Exact identifier application number: M012
ONESSIP DAY TIME KIDS COLD AND COUGH PLUS FEVER	ACETAMINOPHEN 325 MG AND DEXTROMETHORPHAN HBR 10 MG ORAL LIQUID DAY TIME KIDS	MEDWISE LIFESCIENCES INC.	51d52ce4-98c4-2b9b-e063-6294a90ade44	2026-05-15	Warnings	Exact identifier application number: M012
Curewell Tussin DM	DEXTROMETHORPHAN, GUAIFENESIN	RMT HEALTH LLC	4fe9ad93-cdc4-b4df-e063-6294a90a90ae	2026-05-15	Warnings	Exact identifier application number: M012
CounterAct Cough Drops Orchard Cherry	MENTHOL	Melaleuca, Inc.	6049842c-d763-4a91-a225-976ed74e1693	2026-05-15	Warnings	Exact identifier application number: M012
CounterAct Cough Drops Honey Lemon	MENTHOL	Melaleuca, Inc.	84ac3489-9d64-401f-ab78-715af4de5440	2026-05-15	Warnings	Exact identifier application number: M012
ALKA SELTZER COLD Cold Flu and Congestion Maximum Strength Day Night Fast Gels	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, DOXYLAMINE SUCCINATE	Bayer HealthCare LLC.	51e03b5b-b05a-07c1-e063-6394a90ab201	2026-05-15	Warnings	Exact identifier application number: M012
Sinus Congestion and Pain Relief Non-Drowsy/Daytime	ACETAMINOPHEN, GUAIFENESIN AND PHENYLEPHRINE HCL	Rite Aid Corporation	38d73a1e-ac78-4f67-9291-bb48ab80306e	2026-05-15	Warnings	Exact identifier application number: M012
Cold and Flu	ACETAMINOPHEN, DEXTROMETHORPHAN HBR	WALMART INC.	071615ba-f50a-4d2a-a358-43140bccce72	2026-05-14	Warnings	Exact identifier application number: M012
Severe Cold and Flu Nighttime Daytime	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL	HyVee Inc	d4bcfabb-a054-4f53-8dc9-d361a03558b8	2026-05-14	Warnings	Exact identifier application number: M012
Cough and Chest Congestion DM Adult	DEXTROMETHORPHAN HBR, GUAIFENESIN	CVS Pharmacy	4444c05a-eba6-4633-b86f-34f455699fa9	2026-05-14	Warnings	Exact identifier application number: M012
Topcare Day Time Cold and Flu	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL	Topco Associates LLC	a88e5b8e-e6dd-4a1c-9628-5861d3205bdb	2026-05-14	Warnings	Exact identifier application number: M012
equate daytime cold and flu	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE	Wal-Mart Stores Inc	69b24c67-cf4b-46d7-a44b-d1917cc876b1	2026-05-14	Warnings	Exact identifier application number: M012
GILTUSS DIABETIC EX	GILTUSS DIABETIC EX	Gil Pharmaceutical Corp	ab7915e7-323a-4fe1-887a-a3bd3f0aac98	2026-05-13	Warnings	Exact identifier application number: M012
Giltuss EX Maximum Strength Expectorant	GILTUSS EX MAXIMUM STRENGTH EXPECTORANT	Gil Pharmaceutical Corp	950db1ca-6936-47f8-a112-e3594d4c922c	2026-05-13	Warnings	Exact identifier application number: M012
Giltuss EX Expectorant	GILTUSS EX EXPECTORANT	Gil Pharmaceutical Corp	3b363fb9-c4d3-446f-927c-f705ffc715b5	2026-05-13	Warnings	Exact identifier application number: M012
Giltuss HBP EX Expectorant	GILTUSS HBP EX EXPECTORANT	Gil Pharmaceutical Corp	31bd6356-27cf-4188-8fd5-9cd9392021ca	2026-05-13	Warnings	Exact identifier application number: M012

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
TC2D6JAD40	DIPHENHYDRAMINE HYDROCHLORIDE	147-24-0	DIPHENHYDRAMINE HYDROCHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1049632	Benadryl 25 MG Oral Tablet	PSN	702f9786-7ce9-43e4-921d-e1db09612127	31
1049630	diphenhydrAMINE HCl 25 MG Oral Tablet	PSN	702f9786-7ce9-43e4-921d-e1db09612127	31
1049632	diphenhydramine hydrochloride 25 MG Oral Tablet [Benadryl]	SBD	702f9786-7ce9-43e4-921d-e1db09612127	31
1049630	diphenhydramine hydrochloride 25 MG Oral Tablet	SCD	702f9786-7ce9-43e4-921d-e1db09612127	31
1049632	Benadryl 25 MG Oral Tablet	SY	702f9786-7ce9-43e4-921d-e1db09612127	31
1049632	Benadryl Allergy Ultratab 25 MG Oral Tablet	SY	702f9786-7ce9-43e4-921d-e1db09612127	31
1049632	Benadryl 25 MG Oral Tablet	PSN	17633c87-ff0f-4fde-ab23-bc43bdc3fa8e	4
1049632	Benadryl 25 MG Oral Tablet	PSN	76433e3c-142c-4704-8b2b-d602f008c377	4
1049630	diphenhydrAMINE HCl 25 MG Oral Tablet	PSN	17633c87-ff0f-4fde-ab23-bc43bdc3fa8e	4
1049630	diphenhydrAMINE HCl 25 MG Oral Tablet	PSN	76433e3c-142c-4704-8b2b-d602f008c377	4
1049632	diphenhydramine hydrochloride 25 MG Oral Tablet [Benadryl]	SBD	17633c87-ff0f-4fde-ab23-bc43bdc3fa8e	4
1049632	diphenhydramine hydrochloride 25 MG Oral Tablet [Benadryl]	SBD	76433e3c-142c-4704-8b2b-d602f008c377	4
1049630	diphenhydramine hydrochloride 25 MG Oral Tablet	SCD	76433e3c-142c-4704-8b2b-d602f008c377	4
1049630	diphenhydramine hydrochloride 25 MG Oral Tablet	SCD	17633c87-ff0f-4fde-ab23-bc43bdc3fa8e	4
1049632	Benadryl 25 MG Oral Tablet	SY	17633c87-ff0f-4fde-ab23-bc43bdc3fa8e	4
1049632	Benadryl 25 MG Oral Tablet	SY	76433e3c-142c-4704-8b2b-d602f008c377	4
1049632	Benadryl Allergy Ultratab 25 MG Oral Tablet	SY	76433e3c-142c-4704-8b2b-d602f008c377	4
1049632	Benadryl Allergy Ultratab 25 MG Oral Tablet	SY	17633c87-ff0f-4fde-ab23-bc43bdc3fa8e	4
1049632	Benadryl 25 MG Oral Tablet	PSN	8d59d121-62a8-c43b-e053-2a95a90a5847	3
1049630	diphenhydrAMINE HCl 25 MG Oral Tablet	PSN	8d59d121-62a8-c43b-e053-2a95a90a5847	3
1049632	diphenhydramine hydrochloride 25 MG Oral Tablet [Benadryl]	SBD	8d59d121-62a8-c43b-e053-2a95a90a5847	3
1049630	diphenhydramine hydrochloride 25 MG Oral Tablet	SCD	8d59d121-62a8-c43b-e053-2a95a90a5847	3
1049632	Benadryl 25 MG Oral Tablet	SY	8d59d121-62a8-c43b-e053-2a95a90a5847	3
1049632	Benadryl Allergy Ultratab 25 MG Oral Tablet	SY	8d59d121-62a8-c43b-e053-2a95a90a5847	3
1049632	Benadryl 25 MG Oral Tablet	PSN	37573ee4-4df8-4909-bbaf-9a7dbe336e8e	2
1049632	Benadryl 25 MG Oral Tablet	PSN	b1c849e5-8003-4fd3-811d-6a927523e353	2
1049630	diphenhydrAMINE HCl 25 MG Oral Tablet	PSN	37573ee4-4df8-4909-bbaf-9a7dbe336e8e	2
1049630	diphenhydrAMINE HCl 25 MG Oral Tablet	PSN	b1c849e5-8003-4fd3-811d-6a927523e353	2
1049632	diphenhydramine hydrochloride 25 MG Oral Tablet [Benadryl]	SBD	37573ee4-4df8-4909-bbaf-9a7dbe336e8e	2
1049632	diphenhydramine hydrochloride 25 MG Oral Tablet [Benadryl]	SBD	b1c849e5-8003-4fd3-811d-6a927523e353	2
1049630	diphenhydramine hydrochloride 25 MG Oral Tablet	SCD	b1c849e5-8003-4fd3-811d-6a927523e353	2
1049630	diphenhydramine hydrochloride 25 MG Oral Tablet	SCD	37573ee4-4df8-4909-bbaf-9a7dbe336e8e	2
1049632	Benadryl 25 MG Oral Tablet	SY	b1c849e5-8003-4fd3-811d-6a927523e353	2
1049632	Benadryl 25 MG Oral Tablet	SY	37573ee4-4df8-4909-bbaf-9a7dbe336e8e	2
1049632	Benadryl Allergy Ultratab 25 MG Oral Tablet	SY	b1c849e5-8003-4fd3-811d-6a927523e353	2
1049632	Benadryl Allergy Ultratab 25 MG Oral Tablet	SY	37573ee4-4df8-4909-bbaf-9a7dbe336e8e	2
1049632	Benadryl 25 MG Oral Tablet	PSN	d3f44425-db82-4569-8ed0-2fe990b23384	1
1049632	Benadryl 25 MG Oral Tablet	PSN	7c8b3e05-bdd5-46d3-8ff4-ea6e1f188549	1
1049632	Benadryl 25 MG Oral Tablet	PSN	f4ff84b3-bb0c-4900-8ba4-6d1b90394782	1
1049630	diphenhydrAMINE HCl 25 MG Oral Tablet	PSN	d3f44425-db82-4569-8ed0-2fe990b23384	1
1049630	diphenhydrAMINE HCl 25 MG Oral Tablet	PSN	7c8b3e05-bdd5-46d3-8ff4-ea6e1f188549	1
1049630	diphenhydrAMINE HCl 25 MG Oral Tablet	PSN	f4ff84b3-bb0c-4900-8ba4-6d1b90394782	1
1049632	diphenhydramine hydrochloride 25 MG Oral Tablet [Benadryl]	SBD	7c8b3e05-bdd5-46d3-8ff4-ea6e1f188549	1
1049632	diphenhydramine hydrochloride 25 MG Oral Tablet [Benadryl]	SBD	d3f44425-db82-4569-8ed0-2fe990b23384	1
1049632	diphenhydramine hydrochloride 25 MG Oral Tablet [Benadryl]	SBD	f4ff84b3-bb0c-4900-8ba4-6d1b90394782	1
1049630	diphenhydramine hydrochloride 25 MG Oral Tablet	SCD	d3f44425-db82-4569-8ed0-2fe990b23384	1
1049630	diphenhydramine hydrochloride 25 MG Oral Tablet	SCD	7c8b3e05-bdd5-46d3-8ff4-ea6e1f188549	1
1049630	diphenhydramine hydrochloride 25 MG Oral Tablet	SCD	f4ff84b3-bb0c-4900-8ba4-6d1b90394782	1
1049632	Benadryl 25 MG Oral Tablet	SY	7c8b3e05-bdd5-46d3-8ff4-ea6e1f188549	1
1049632	Benadryl 25 MG Oral Tablet	SY	d3f44425-db82-4569-8ed0-2fe990b23384	1
1049632	Benadryl 25 MG Oral Tablet	SY	f4ff84b3-bb0c-4900-8ba4-6d1b90394782	1
1049632	Benadryl Allergy Ultratab 25 MG Oral Tablet	SY	d3f44425-db82-4569-8ed0-2fe990b23384	1
1049632	Benadryl Allergy Ultratab 25 MG Oral Tablet	SY	f4ff84b3-bb0c-4900-8ba4-6d1b90394782	1
1049632	Benadryl Allergy Ultratab 25 MG Oral Tablet	SY	7c8b3e05-bdd5-46d3-8ff4-ea6e1f188549	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
50580-226-12	50580022612	1 BLISTER PACK in 1 CARTON (50580-226-12) / 12 TABLET, FILM COATED in 1 BLISTER PACK	1 blister pack	2025-06-11		No	No	Current
50580-226-20	50580022620	2 CARTON in 1 CARTON (50580-226-20) / 1 BOTTLE in 1 CARTON / 100 TABLET, FILM COATED in 1 BOTTLE	2 carton	2024-01-15		No	No	Current
50580-226-33	50580022633	3 CARTON in 1 CARTON (50580-226-33) / 1 BOTTLE in 1 CARTON / 48 TABLET, FILM COATED in 1 BOTTLE	3 carton	2025-07-28		No	No	Current
50580-226-50	50580022650	1 BOTTLE in 1 CARTON (50580-226-50) / 100 TABLET, FILM COATED in 1 BOTTLE	1 bottle	2012-06-04	0000-00-00	No	No	Current
50580-226-51	50580022651	2 BLISTER PACK in 1 CARTON (50580-226-51) / 12 TABLET, FILM COATED in 1 BLISTER PACK	2 blister pack	2012-06-04	0000-00-00	No	No	Current
50580-226-52	50580022652	4 BLISTER PACK in 1 CARTON (50580-226-52) / 12 TABLET, FILM COATED in 1 BLISTER PACK	4 blister pack	2012-06-04	0000-00-00	No	No	Current
50580-226-53	50580022653	2 TABLET, FILM COATED in 1 POUCH (50580-226-53)		2012-06-04	0000-00-00	No	No	Current
50580-226-54	50580022654	60 POUCH in 1 CARTON (50580-226-54) / 2 TABLET, FILM COATED in 1 POUCH	60 pouch	2015-07-27	0000-00-00	No	No	Current
50580-226-56	50580022656	3 CARTON in 1 PACKAGE (50580-226-56) / 4 BLISTER PACK in 1 CARTON / 12 TABLET, FILM COATED in 1 BLISTER PACK	3 carton	2013-02-01	0000-00-00	No	No	Current
50580-226-62	50580022662	4 POUCH in 1 CARTON (50580-226-62) / 2 TABLET, FILM COATED in 1 POUCH	4 pouch	2017-01-02	0000-00-00	No	No	Current
50580-226-70	50580022670	1 BOTTLE in 1 CARTON (50580-226-70) / 48 TABLET, FILM COATED in 1 BOTTLE	1 bottle	2025-06-02		No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Benadryl ®	Kenvue Brands LLC	2026-07-28	HUMAN OTC DRUG LABEL	32
Benadryl ®	Select Consumer Group	2026-07-04	HUMAN OTC DRUG LABEL	1
Benadryl Allergy Ultratab	Savings Distributors LLC	2026-05-01	HUMAN OTC DRUG LABEL	3
Benadryl Allergy	JC World Bell Wholesale Co., Inc.	2025-09-03	HUMAN OTC DRUG LABEL	1
Benadryl ®	Morning Star OTC	2025-06-09	HUMAN OTC DRUG LABEL	1
Benadryl Ultra Tab	JC World Bell Wholesale Co., Inc. \| Kenvue Brands LLC	2024-12-31	HUMAN OTC DRUG LABEL	4
Benadryl Ultratabs	Navajo Manufacturing Company Inc.	2024-10-02	HUMAN OTC DRUG LABEL	4
Benadryl ®	Proficient Rx LP	2023-12-01	HUMAN OTC DRUG LABEL	2
Benadryl ®	REMEDYREPACK INC.	2022-09-22	HUMAN OTC DRUG LABEL	5
Benadryl ®	Select Corporation	2022-03-30	HUMAN OTC DRUG LABEL	1
Benadryl ®	Central Texas Community Health Centers \| Travis County Healthcare District	2018-09-24	HUMAN OTC DRUG LABEL	2