allergy

Product NDC: 56062-479
11-digit product format: 560620479
Labeler code: 56062
Product ID: 56062-479_d0b0bff2-487d-4fe0-a933-3ca2c6d07596
Type: HUMAN OTC DRUG
Nonproprietary name: Diphenhydramine Hydrochloride
Dosage form: TABLET
Route: ORAL
Labeler: Publix Super Markets Inc
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 1998-05-07
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: 2026-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	56062-479	56062-479-62	D	Discontinued by firm		2026-10-21
excluded package	package	56062-479	56062-479-67	D	Discontinued by firm		2026-10-21

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 · 20 matching rows.

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

Captured / source date, Package NDC, Snapshot table
Captured / source date	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	56062-479-62	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	56062-479-67	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	56062-479-62	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	56062-479-67	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	56062-479-62	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	56062-479-67	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	56062-479-62	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	56062-479-67	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	56062-479-62	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	56062-479-67	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	56062-479-62	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	56062-479-67	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	56062-479-62	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	56062-479-67	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	56062-479-62	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	56062-479-67	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	56062-479-62	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	56062-479-67	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	56062-479-67	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	56062-479-67	`367a005e9d99…`	`383a685ebd0f…`

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: allergy
Listing expiration: 2026-12-31

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 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1049630	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
23a98385-28cc-4fac-8c87-b3ced8106532	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, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
56062-479-62	2024-01-30	C162847	48780-1	1030e365-4f94-111a-e063-dadaa90a10e2	Publix Super Markets, Inc. Allergy Tablets Drug Facts
56062-479-67	2024-01-30	C162847	48780-1	1030e365-4f94-111a-e063-dadaa90a10e2	Publix Super Markets, Inc. Allergy Tablets Drug Facts
56062-479-78	2024-01-30	C162847	48780-1	1030e365-4f94-111a-e063-dadaa90a10e2	Publix Super Markets, Inc. Allergy Tablets Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
56062-479-62	allergy	24 in 1 CARTON	TABLET	24	7
56062-479-62	allergy	1 in 1 BLISTER PACK	TABLET	1	7
56062-479-67	allergy	1 in 1 BLISTER PACK	TABLET	1	7
56062-479-67	allergy	48 in 1 CARTON	TABLET	48	7
56062-479-78	allergy	100 in 1 BOTTLE	TABLET	100	7
56062-479-78	allergy	1 in 1 CARTON	TABLET	1	7

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
56062-479-62	EA - Each	56062-479	d2cf61c4-ba45-4d60-9400-745f0775349b	1	2013-09-04
56062-479-67	EA - Each	56062-479	442a691a-7f8c-41a7-9d18-739a879f46ed	1	2013-09-04
56062-479-78	EA - Each	56062-479	5d6e0869-6e01-4fd8-8d13-9b794e22969d	1	2013-09-04

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
DIPHENHYDRAMINE HYDROCHLORIDE	ACTIVE INGREDIENT	TC2D6JAD40	ALLERGY (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [PUBLIX SUPER MARKETS INC]	3
DIPHENHYDRAMINE	ACTIVE MOIETY	8GTS82S83M	ALLERGY (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [PUBLIX SUPER MARKETS INC]	3
CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE	INACTIVE INGREDIENT	O7TSZ97GEP	ALLERGY (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [PUBLIX SUPER MARKETS INC]	3
CARNAUBA WAX	INACTIVE INGREDIENT	R12CBM0EIZ	ALLERGY (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [PUBLIX SUPER MARKETS INC]	3
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	ALLERGY (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [PUBLIX SUPER MARKETS INC]	3
CROSPOVIDONE	INACTIVE INGREDIENT	68401960MK	ALLERGY (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [PUBLIX SUPER MARKETS INC]	3
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	ALLERGY (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [PUBLIX SUPER MARKETS INC]	3
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	ALLERGY (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [PUBLIX SUPER MARKETS INC]	3
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	ALLERGY (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [PUBLIX SUPER MARKETS INC]	3
POLYSORBATE 80	INACTIVE INGREDIENT	6OZP39ZG8H	ALLERGY (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [PUBLIX SUPER MARKETS INC]	3
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	ALLERGY (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [PUBLIX SUPER MARKETS INC]	3
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	ALLERGY (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [PUBLIX SUPER MARKETS INC]	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
56062-479	ALLERGY (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [PUBLIX SUPER MARKETS INC]	7	Current NDC, Legacy NDC, 6 package rows	20240722_23a98385-28cc-4fac-8c87-b3ced8106532.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 88 of 178 · 3,551 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MULTI-SYMPTOM COLD	DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL	Family Dollar Services Inc	b1fae7cc-4033-44bc-aa7c-ca3ceea51c7d	2025-11-15	Warnings	Exact identifier application number: M012
Cold and Flu Severe	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL	Rite Aid Corporation	1affbef6-dd27-40c2-a5d3-b121aa62496a	2025-11-15	Warnings	Exact identifier application number: M012
Cold and Flu Day, Night	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL	Walgreen Company	b9adfb5d-6576-4ff8-a7d7-a89b867c5292	2025-11-14	Warnings	Exact identifier application number: M012
PECGEN DMX	DEXTROMETHORPHAN HBR, GUAIFENESIN	KRAMER NOVIS	a627824c-5e3d-4672-a047-6c801b50b432	2025-11-14	Warnings	Exact identifier application number: M012
Supress DM	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN	KRAMER NOVIS	7da0611e-729c-4cf8-88f3-f8877b9f5cfa	2025-11-14	Warnings	Exact identifier application number: M012
G-ZYNCOF	DEXTROMETHORPHAN HBR AND GUAIFENESIN	Kramer Novis	c1aa7060-0f32-4ea1-8e2e-1aa131bd55fc	2025-11-14	Warnings	Exact identifier application number: M012
equate vapor ice cold and flu	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE	Wal-Mart Stores Inc	b2c0692c-ed0b-4fcf-b88d-59a788b124c6	2025-11-14	Warnings	Exact identifier application number: M012
Guaifenesin 400mg	GUAIFENESIN	Marlex Pharmaceuticals Inc	13f4db4e-687e-9d7b-e063-6294a90ab088	2025-11-13	Warnings	Exact identifier application number: M012
Guaifenesin 200mg	GUAIFENESIN	Marlex Pharmaceuticals Inc	13b8f480-d1ac-d70c-e063-6394a90ab4f4	2025-11-13	Warnings	Exact identifier application number: M012
Diphenhydramine HCL	DIPHENHYDRAMINE HCL	PD-Rx Pharmaceuticals, Inc.	c1873a4c-661f-4896-bcc0-f6d3a655de94	2025-11-13	Warnings	Exact identifier application number: M012
Theraflu Severe Cold Relief Nighttime	ACETAMINOPHEN, DIPHENHYDRAMINE HCL	Haleon US Holdings LLC	c24b9489-208c-472b-8ae5-c6e86c12e04d	2025-11-13	Warnings	Exact identifier application number: M012
Theraflu Severe Cold Relief Chest Congestion Daytime	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN	Haleon US Holdings LLC	8c821671-dc68-4e27-aa87-b4e45ade9817	2025-11-13	Warnings	Exact identifier application number: M012
Robitussin Maximum Strength Severe Cough Plus Sore Throat	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE	Haleon US Holdings LLC	6a6f5da8-6433-4284-8df7-2d5b099b74dc	2025-11-13	Warnings	Exact identifier application number: M012
equaline allergy	DIPHENHYDRAMINE HCL	United Natural Foods, Inc. dba UNFI	8e4eb1eb-5b55-4531-94d2-998425ec80ed	2025-11-13	Warnings	Exact identifier application number: M012
Cold and Flu DayTime	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE	Safeway, Inc.	7a78f24b-7c23-4318-99dc-90c05db185b1	2025-11-13	Warnings	Exact identifier application number: M012
ZYNCOF	DEXTROMETHORPHAN HBR AND GUAIFENESIN	Kramer Novis	cffd6d5f-0cb2-4d38-bdb0-6a21120418cc	2025-11-13	Warnings	Exact identifier application number: M012
equate vapor ice cold and flu	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE	Wal-Mart Stores Inc	b6da1659-8c79-4cce-a817-907a7f061a2d	2025-11-13	Warnings	Exact identifier application number: M012
Tussi Pres	GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDE	Kramer Novis	0d4ee530-2a5c-41a0-88bf-ac92d538661b	2025-11-12	Warnings	Exact identifier application number: M012
4 Way Fast Acting	PHENYLEPHRINE HYDROCHLORIDE	Haleon US Holdings LLC	a8fc41c7-4425-41b8-b1c6-eb22ac054734	2025-11-12	Warnings	Exact identifier application number: M012
Quality Choice Vapor Steam	CAMPHOR (SYNTHETIC)	Chain Drug Marketing Association, Inc.	1f1e6be5-d407-330c-e063-6294a90a4e80	2025-11-12	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
1049630	diphenhydrAMINE HCl 25 MG Oral Tablet	PSN	23a98385-28cc-4fac-8c87-b3ced8106532	7
1049630	diphenhydramine hydrochloride 25 MG Oral Tablet	SCD	23a98385-28cc-4fac-8c87-b3ced8106532	7

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
56062-479-62	56062047962	24 BLISTER PACK in 1 CARTON (56062-479-62) > 1 TABLET in 1 BLISTER PACK	24 blister pack	1998-05-07	0000-00-00	No	No	Current
56062-479-67	56062047967	48 BLISTER PACK in 1 CARTON (56062-479-67) > 1 TABLET in 1 BLISTER PACK	48 blister pack	2002-04-18	0000-00-00	No	No	Current
56062-479-78	56062047978	1 BOTTLE in 1 CARTON (56062-479-78) / 100 TABLET in 1 BOTTLE	1 bottle	2007-11-26	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Publix Super Markets, Inc. Allergy Tablets Drug Facts	Publix Super Markets Inc	2024-07-16	HUMAN OTC DRUG LABEL	7