Allergy Relief

Product NDC
21130-329
11-digit product format
211300329
Labeler code
21130
Product ID
21130-329_61f378b4-cb32-4a07-ad4c-eabb04629ba4
Type
HUMAN OTC DRUG
Nonproprietary name
Diphenhydramine HCl
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Better Living Brands, LLC
Application
M012
Marketing category
OTC MONOGRAPH DRUG
Marketing start
1990-03-02
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

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 · 3 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage21130-32921130-329-06DDiscontinued by firm2026-10-21
excluded packagepackage21130-32921130-329-12DDiscontinued by firm2026-10-21
excluded packagepackage21130-32921130-329-22DDiscontinued by firm2026-10-21

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 Relief
Listing expiration
2027-12-31

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
65802aa7-64e7-4435-ad6b-65895fba17ceAvailable 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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21130-329-06Allergy Relief1 in 1 CARTONTABLET, FILM COATED120
21130-329-06Allergy Relief200 in 1 BOTTLE, PLASTICTABLET, FILM COATED20020
21130-329-08Allergy Relief12 in 1 BLISTER PACKTABLET, FILM COATED1220
21130-329-08Allergy Relief2 in 1 CARTONTABLET, FILM COATED220
21130-329-12Allergy Relief1 in 1 CARTONTABLET, FILM COATED120
21130-329-12Allergy Relief100 in 1 BOTTLE, PLASTICTABLET, FILM COATED10020
21130-329-22Allergy Relief4 in 1 CARTONTABLET, FILM COATED420
21130-329-22Allergy Relief12 in 1 BLISTER PACKTABLET, FILM COATED1220

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21130-329ALLERGY RELIEF (DIPHENHYDRAMINE HCL) TABLET, FILM COATED [BETTER LIVING BRANDS, LLC]19Current NDC, Legacy NDC, 8 package rows20240718_65802aa7-64e7-4435-ad6b-65895fba17ce.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 98 of 178 · 3,551 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
EquateVAPORIZING STEAM LIQUIDWalmart Inc.ffede19a-06e2-61c7-e053-6394a90ac77b2025-10-08WarningsExact identifier
application number: M012
Menthol Drops Dollar General Severe Honey Lemon 45ctMENTHOLDollar General Corporation0ea61a4c-690a-4349-9952-cc17fb1f06712025-10-08WarningsExact identifier
application number: M012
Cough Drops Dollar General Menthol 30ctMENTHOLDollar General Corporation892092cc-5a1c-4309-baf9-a040888d35772025-10-08WarningsExact identifier
application number: M012
Cough Drops Dollar General Menthol 80ctMENTHOLDollar General Corporation773f4ad2-6c91-431f-ad3d-c0e53e7ca9182025-10-08WarningsExact identifier
application number: M012
Menthol Drops Dollar General Severe 45ctMENTHOLDollar General Corporation13c7d3b1-12ac-4931-877c-728d3d89942c2025-10-08WarningsExact identifier
application number: M012
Menthol Drops Dollar General Severe Honey Lemon 45ctMENTHOLDollar General Corporationd0c878f0-a737-4583-9847-834af70e7d6f2025-10-08WarningsExact identifier
application number: M012
Cough Drops Freegells Strawberry 30ctMENTHOLR.L. ALBERT & SON, INCdc077c36-c403-4b83-894a-e9922e9288412025-10-08WarningsExact identifier
application number: M012
Cough Drops Freegells Strawberry 30ctMENTHOLRL Albert & Son Inc.2ea760f3-df50-4c46-a43d-d5ed07f421a52025-10-08WarningsExact identifier
application number: M012
Freegells Cough Drops Honey Lemon 200ctMENTHOLRL Albert & Son Inc.3ac08274-08d9-4dab-b09a-6e297948a25a2025-10-08WarningsExact identifier
application number: M012
Freegells Cough Drops Honey Lemon 30ctMENTHOLRL Albert & Son Inc.8114e1a2-728d-4489-a494-f28a5e7d9bb32025-10-08WarningsExact identifier
application number: M012
Freegells Cough Drops Menthol 30ctMENTHOLRL Albert & Son Inc.0c2e594a-cdf8-4595-bda6-0ebc19ac38502025-10-08WarningsExact identifier
application number: M012
Freegells Cough Drops Menthol Cherry 200ctMENTHOLR.L. ALBERT & SON, INCf62b7f75-3275-46c9-880c-64148d0dce592025-10-08WarningsExact identifier
application number: M012
Freegells Cough Drops Menthol 80ctMENTHOLR.L. ALBERT & SON, INC15917bfb-f660-4a12-bdcc-5b4a96e0e1d02025-10-08WarningsExact identifier
application number: M012
Freegells Cough Drops Menthol Cherry 30ctMENTHOLRL Albert & Son Inc.92c54c53-c8bb-4576-abae-715a2f3878bf2025-10-08WarningsExact identifier
application number: M012
Freegells Cough Drops Menthol 80ctMENTHOLRL Albert & Son Inc.c96cc162-5908-4990-9dc1-3ce9128442742025-10-08WarningsExact identifier
application number: M012
Freegells Cough Drops Menthol Cherry 30ctMENTHOLR.L. ALBERT & SON, INCbac77712-6197-4b30-a5f8-9b99eb9d7b5a2025-10-08WarningsExact identifier
application number: M012
Freegells Cough Drops Menthol Cherry 80ctMENTHOLR.L. ALBERT & SON, INC6842d766-ade6-40b2-831b-f4feac25c6db2025-10-08WarningsExact identifier
application number: M012
Freegells Cough Drops Menthol Cherry 80ctMENTHOLRL Albert & Son Inc.9f324ca1-0e2a-47e3-997e-2aaa68a857512025-10-08WarningsExact identifier
application number: M012
Freegells Cough Drops Menthol Honey Lemon 30ctMENTHOLR.L. ALBERT & SON, INC2063a013-aa0b-465d-b04f-cfe2e70d749f2025-10-08WarningsExact identifier
application number: M012
Freegells Cough Drops Menthol Honey Lemon 200ctMENTHOLR.L. ALBERT & SON, INCcd81488c-74d8-48d9-9c73-ff662a5cd4cd2025-10-08WarningsExact identifier
application number: M012

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1049630diphenhydrAMINE HCl 25 MG Oral TabletPSN65802aa7-64e7-4435-ad6b-65895fba17ce20
1049630diphenhydramine hydrochloride 25 MG Oral TabletSCD65802aa7-64e7-4435-ad6b-65895fba17ce20

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
21130-329-06211300329061 BOTTLE in 1 CARTON (21130-329-06) > 200 TABLET in 1 BOTTLE1 bottle1990-03-020000-00-00NoNoCurrent
21130-329-08211300329082 BLISTER PACK in 1 CARTON (21130-329-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK2 blister pack1990-03-020000-00-00NoNoCurrent
21130-329-12211300329121 BOTTLE, PLASTIC in 1 CARTON (21130-329-12) > 100 TABLET in 1 BOTTLE, PLASTIC1990-03-020000-00-00NoNoCurrent
21130-329-22211300329224 BLISTER PACK in 1 CARTON (21130-329-22) > 12 TABLET in 1 BLISTER PACK4 blister pack1990-03-020000-00-00NoNoCurrent