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 92 of 177 · 3,534 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Family Care Saline	SODIUM CHLORIDE	United Exchange Corp.	06737393-d4ae-3e7b-e063-6394a90ac19f	2025-10-31	Warnings	Exact identifier application number: M012
QUALITY CHOICE Maximum Strength Daytime Cold and Flu	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE	Chain Drug Marketing Association, Inc.	40416ff5-06e1-97dd-e063-6394a90a2046	2025-10-30	Warnings	Exact identifier application number: M012
Robitussin Maximum Strength Nighttime Cough DM	DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE	Haleon US Holdings LLC	44feee2f-25bc-48d4-8e13-db1d9daaaa90	2025-10-30	Warnings	Exact identifier application number: M012
Robitussin Day and Night Cough Relief DM Max	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, DOXYLAMINE SUCCINATE	Haleon US Holdings LLC	b3d02c91-8f79-4eb4-a378-1072474c572c	2025-10-30	Warnings	Exact identifier application number: M012
ROBITUSSIN MAXIMUM STRENGTH COUGH PLUS CHEST CONGESTION DM	DEXTROMETHORPHAN HBR, GUAIFENESIN	Haleon US Holdings LLC	f1d022dd-c2ca-497f-87d5-9ef3e20e8ea7	2025-10-30	Warnings	Exact identifier application number: M012
Endal	TRIPROLIDINE HCL, DEXTROMETHORPHAN HBR	Poly Pharmaceuticals, Inc.	fc5401e2-ed65-72e7-e053-6294a90a81f3	2025-10-30	Warnings	Exact identifier application number: M012
daytime	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL	Publix Super Markets Inc	c7cef266-46fc-49ab-a2e7-54fc56298659	2025-10-30	Warnings	Exact identifier application number: M012
Allergy Relief	DIPHENHYDRAMINE HYDROCHLORIDE	SAM'S WEST INC	16592ad7-b7cb-0837-e063-6394a90ae059	2025-10-29	Warnings	Exact identifier application number: M012
Maximum Strength Severe Congestion and Cough	DEXTROMETHORPHAN HBR, GUAIFENESIN, AND PHENYLEPHRINE HCL	SAFEWAY	013b94a1-26c7-4371-981a-d1b9d7fd1c98	2025-10-29	Warnings	Exact identifier application number: M012
Better Living	PHENYLEPHRINE HYDROCHLORIDE	BETTER LIVING BRANDS LLC	aea0db7f-e01a-4d8e-9c20-4a5ef4a905d1	2025-10-29	Warnings	Exact identifier application number: M012
AXIM DayTime - Night Time 72 Softgels	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE	VIVUNT PHARMA LLC	de9eb2d5-ba51-4637-e053-2995a90a0451	2025-10-29	Warnings	Exact identifier application number: M012
Dollar General Vapor Steam	CAMPHOR (SYNTHETIC)	DOLGENCORP, LLC	86d0f3ac-1359-c2f9-e053-2a91aa0a35d0	2025-10-29	Warnings	Exact identifier application number: M012
Maximum Strength Mucus Relief DM	DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN	Wal-Mart Stores,Inc.,	a748d5ab-901c-47bb-8437-997542ecebfe	2025-10-28	Warnings	Exact identifier application number: M012
Nighttime Childrens Multi Symptoms Cold and Cough Multi-Symptom Relief	CHLORPHENIRAMINE MALEATE AND DEXTROMETHORPHAN HYDROBROMIDE	WAL-MART STORES,INC.	68a68574-0fcb-4569-be57-d9aee5f62bea	2025-10-28	Warnings	Exact identifier application number: M012
Maximum Strength Mucus Relief Severe Congestion and Cough	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	Wal-Mart Stores,Inc.,	635009a1-6154-4c62-a4be-d4f32c2cef8d	2025-10-28	Warnings	Exact identifier application number: M012
Family Care Nasal Relief	OXYMETAZOLINE HYDROCHLORIDE	United Exchange Corp	6d0f8e9e-0503-522b-e053-2a91aa0aca35	2025-10-28	Warnings	Exact identifier application number: M012
Family Care Nasal Relief	OXYMETAZOLINE HYDROCHLORIDE	United Exchange Corp	6d0eef2f-f546-d769-e053-2991aa0a8fe4	2025-10-28	Warnings	Exact identifier application number: M012
Tussin DM Cough and Chest Congestion Adult	DEXTROMETHORPHAN HBR, GUAIFENESIN	P & L Development, LLC	4af67ba7-8892-442c-b9fb-80aba9140e05	2025-10-28	Warnings	Exact identifier application number: M012
No Drip Nasal Mist Nasal Decongestant Severe Congestion	OXYMETAZOLINE HYDROCHLORIDE	Wal-Mart Stores,Inc.,	994fa270-65bb-4097-b88a-d5ce3c0e1c79	2025-10-27	Warnings	Exact identifier application number: M012
Dye Free Childrens Allergy Relief	DIPHENHYDRAMINE HYDROCHLORIDE	WAL-MART STORES INC.	3652ee94-b762-4100-a305-5acbec5f795a	2025-10-27	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