good sense allergy relief

Product NDC
0113-0479
11-digit product format
001130479
Labeler code
0113
Product ID
0113-0479_9f4c73e7-71c5-4a82-819b-a39ee74f4145
Type
HUMAN OTC DRUG
Nonproprietary name
Diphenhydramine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
L. Perrigo Company
Application
M012
Marketing category
OTC MONOGRAPH DRUG
Marketing start
1991-08-20
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
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage0113-04790113-0479-53DDiscontinued by firm2026-10-15
excluded packagepackage0113-04790113-0479-67DDiscontinued by firm2026-10-15

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 · 24 matching rows.

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

Captured / source date, Package NDC, Snapshot table
Captured / source datePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-050113-0479-53d630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-050113-0479-67d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-260113-0479-53f5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-260113-0479-67f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-310113-0479-532ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-310113-0479-672ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-280113-0479-53a1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-280113-0479-67a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-210113-0479-53cfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-210113-0479-67cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-100113-0479-53cdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-100113-0479-67cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-310113-0479-53302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-310113-0479-67302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-200113-0479-53ed331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-200113-0479-67ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100113-0479-530efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-100113-0479-670efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-080113-0479-53ad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-080113-0479-67ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-030113-0479-53367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-030113-0479-67367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-090113-0479-53557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-090113-0479-67557ba5c1ecfa…9c80585c8c6e…

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
good sense allergy relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DIPHENHYDRAMINE HYDROCHLORIDE25 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
TC2D6JAD40Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1049630Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
2cfa69b4-e33f-442a-a6df-b021b041da14Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0e2e0f88-b076-afe1-4bdd-32bca4375becProduct name320250127
3e48c9c4-918d-5d23-2f0b-d2398b06be54Product name120140508
865c72dd-0d94-daac-f728-ddd4ded2a79eProduct name120140508

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0113-0479-53good sense allergy relief1 in 1 BLISTER PACKTABLET19
0113-0479-53good sense allergy relief12 in 1 CARTONTABLET129
0113-0479-62good sense allergy relief24 in 1 CARTONTABLET249
0113-0479-62good sense allergy relief1 in 1 BLISTER PACKTABLET19
0113-0479-67good sense allergy relief48 in 1 CARTONTABLET489
0113-0479-67good sense allergy relief1 in 1 BLISTER PACKTABLET19
0113-0479-78good sense allergy relief100 in 1 BOTTLETABLET1009
0113-0479-78good sense allergy relief1 in 1 CARTONTABLET19
0113-0479-79good sense allergy relief400 in 1 BOTTLETABLET4009

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0113-0479-53EA - Each0113-0479ee7a9bd6-c9e5-4049-a57f-f0df7b23a1c912018-02-20
0113-0479-62EA - Each0113-04798f6a54c4-4fa6-4bf7-a24a-10810f8a4ac412013-02-13
0113-0479-78EA - Each0113-0479d935c09b-7aa6-4a73-a496-1316061e792112013-02-13
0113-0479-79EA - Each0113-04794a7a8732-c938-489c-a655-e838ed92030012020-09-14

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
DIPHENHYDRAMINE HYDROCHLORIDEACTIVE INGREDIENTTC2D6JAD40GOOD SENSE ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [L. PERRIGO COMPANY]2
DIPHENHYDRAMINEACTIVE MOIETY8GTS82S83MGOOD SENSE ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [L. PERRIGO COMPANY]2
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUSINACTIVE INGREDIENTL11K75P92JGOOD SENSE ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [L. PERRIGO COMPANY]2
CARNAUBA WAXINACTIVE INGREDIENTR12CBM0EIZGOOD SENSE ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [L. PERRIGO COMPANY]2
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UGOOD SENSE ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [L. PERRIGO COMPANY]2
CROSPOVIDONEINACTIVE INGREDIENT68401960MKGOOD SENSE ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [L. PERRIGO COMPANY]2
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOGOOD SENSE ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [L. PERRIGO COMPANY]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30GOOD SENSE ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [L. PERRIGO COMPANY]2
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1AGOOD SENSE ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [L. PERRIGO COMPANY]2
POLYSORBATE 80INACTIVE INGREDIENT6OZP39ZG8HGOOD SENSE ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [L. PERRIGO COMPANY]2
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65APGOOD SENSE ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [L. PERRIGO COMPANY]2
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPGOOD SENSE ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [L. PERRIGO COMPANY]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0113-0479GOOD SENSE ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [L. PERRIGO COMPANY]9Current NDC, Legacy NDC, 9 package rows20240202_2cfa69b4-e33f-442a-a6df-b021b041da14.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 5 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MUCUS RELIEFGUAIFENESINGeri-Care Pharmaceuticals, Corp5afb242f-fac9-dc81-e063-6394a90a84482026-08-27WarningsExact identifier
application number: M012
daytime cold and fluACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDEAmazon.com Services LLC6de619d3-0ab0-43e7-8dac-7bbd5368ac652026-08-27WarningsExact identifier
application number: M012
Daytime Mucus Relief Severe Congestion and Cough and Nighttime Cold and Flu Maximum StrengthDEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCI, ACETAMINOPHEN, DIPHENHYDRAMINE HCIWalgreens366ddac8-9e8a-41bd-a7f7-48213485a5f82026-08-27WarningsExact identifier
application number: M012
Nighttime Cold and Flu Maximum StrengthACETAMINOPHEN, DIPHENHYDRAMINE HCI, PHENYLEPHRINE HCIWalgreens37896933-3ed3-457f-8a32-ee0d784a19e82026-08-27WarningsExact identifier
application number: M012
Allergy ReliefDIPHENHYDRAMINE HYDROCHLORIDEAmazon.com Services LLC298e9164-e378-4b39-a944-bfc8f8baa4de2026-08-27WarningsExact identifier
application number: M012
DayTime Mucus Relief Severe Cold and Nighttime Cold and Flu Maximum StrengthDAYTIME ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCI, NIGHTTIME ACETAMINOPHEN, DIPHENHYDRAMINE HCI, PHENYLEPHRINE HCIWalgreens3b4b3b04-eff9-4e06-8b37-f6729671d07f2026-08-27WarningsExact identifier
application number: M012
Daytime Cold and Flu mini SoftgelsACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCLShield Pharmaceuticals Corpdfb0fe2e-b0c7-409a-bd1a-fd12485665ba2026-08-26WarningsExact identifier
application number: M012
Nighttime Severe Cold and Flu Maximum Strength mini softgelsACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCLShield Pharmaceuticals Corp70c5517d-be4e-4317-b4f4-df660c71c6992026-08-26WarningsExact identifier
application number: M012
Cold and FluACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCLMeijer Distribution, Inc.c1f9ec75-7eb2-405c-8cdc-097cbf2cf87d2026-08-26WarningsExact identifier
application number: M012
Childrens TYLENOL COLD plus COUGH plus RUNNY NOSEACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, AND DEXTROMETHORPHAN HYDROBROMIDEKenvue Brands LLC5b95905e-b729-4caf-921a-fc4ef815289c2026-08-25WarningsExact identifier
application number: M012
Allergy ReliefDIPHENHYDRAMINE HCLWal-Mart Stores Incc88e93d4-66b6-4327-b9e5-0e0a95a18d662026-08-25WarningsExact identifier
application number: M012
Sleep Aid NightTimeDIPHENHYDRAMINE HCLDolgencorp, Inc. (DOLLAR GENERAL & REXALL)4fff664b-4ff0-4007-95ab-cb273807b9b42026-08-25WarningsExact identifier
application number: M012
Allergy ReliefDIPHENHYDRAMINE HCLWalgreen Company7d972559-6184-476b-9cbf-1bc5663ea00d2026-08-24WarningsExact identifier
application number: M012
Cold, Flu and Sore ThroatACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCLMeijer Distribution, Inc.9be8437c-6053-4ed4-bdd2-97f556b5289e2026-08-24WarningsExact identifier
application number: M012
Extra Strength Tylenol Cold Plus Flu Multi-Symptom Day NightACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, CHLORPHENIRAMINE MALEATEKenvue Brands LLC594f515c-b369-816d-e063-6294a90a59a12026-08-21WarningsExact identifier
application number: M012
DG HEALTH MULTI SYMPTOM SEVERE COLDACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCLDolgencorp, LLC47ddbb0d-0823-4817-9c56-e7fff77d601c2026-08-21WarningsExact identifier
application number: M012
Mucus Relief DM MaxDEXTROMETHORPHAN HBR, GUAIFENESINDOLGENCORP, LLC5be4e730-3cd6-414e-a23b-f6cad80887502026-08-21WarningsExact identifier
application number: M012
Mucus Relief DM Cough Maximum StrengthDEXTROMETHORPHAN HBR AND GUAIFENESINCardinal Health 110, LLC. DBA Leader6304a581-9238-4539-b157-293fc05c173e2026-08-21WarningsExact identifier
application number: M012
COMBINATION PACK HyVee Daytime and Nighttime Severe Cold and Flu SOFTGEL - 24ctACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, DOXYLAMINE SUCCINATEHyVee Inc82ead335-d38e-40c3-8031-222bf985a3022026-08-20WarningsExact identifier
application number: M012
HyVee Nighttime Severe Cold and Flu SOFTGELACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDEHyVee Inc49818610-bf4a-fb86-e063-6294a90ae5982026-08-20WarningsExact identifier
application number: M012

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1049630diphenhydrAMINE HCl 25 MG Oral TabletPSN2cfa69b4-e33f-442a-a6df-b021b041da149
1049630diphenhydramine hydrochloride 25 MG Oral TabletSCD2cfa69b4-e33f-442a-a6df-b021b041da149
1049630diphenhydrAMINE HCl 25 MG Oral TabletPSN4d0f4f5b-3135-4457-bb8f-ad9d28ca5ea45
1049630diphenhydramine hydrochloride 25 MG Oral TabletSCD4d0f4f5b-3135-4457-bb8f-ad9d28ca5ea45

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0113-0479-530011304795312 BLISTER PACK in 1 CARTON (0113-0479-53) > 1 TABLET in 1 BLISTER PACK12 blister pack2016-08-100000-00-00NoNoCurrent
0113-0479-620011304796224 BLISTER PACK in 1 CARTON (0113-0479-62) / 1 TABLET in 1 BLISTER PACK24 blister pack1991-08-200000-00-00NoNoCurrent
0113-0479-670011304796748 BLISTER PACK in 1 CARTON (0113-0479-67) > 1 TABLET in 1 BLISTER PACK48 blister pack2021-06-040000-00-00NoNoCurrent
0113-0479-78001130479781 BOTTLE in 1 CARTON (0113-0479-78) / 100 TABLET in 1 BOTTLE1 bottle1993-10-060000-00-00NoNoCurrent
0113-0479-7900113047979400 TABLET in 1 BOTTLE (0113-0479-79) 400 tablet2001-02-260000-00-00NoNoCurrent