FDA.reportPublic FDA data

Benadryl Ultratabs

Product NDC
67751-166
11-digit product format
677510166
Labeler code
67751
Product ID
67751-166_2385ad34-3763-390b-e063-6394a90a12fd
Type
HUMAN OTC DRUG
Nonproprietary name
DIPHENHYDRAMINE HYDROCHLORIDE
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Navajo Manufacturing Company Inc.
Application
M012
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2016-09-22
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

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 Ultratabs
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 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1049630Internal RxNorm lookup
1049632Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
76433e3c-142c-4704-8b2b-d602f008c377Available 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#

NDC, Effective, Related label table
NDCEffectiveRelated label
67751-166-012023-03-15Benadryl Ultratabs
67751-166-022023-03-15Benadryl Ultratabs
67751-166-012023-01-30Benadryl Ultratabs
67751-166-022023-01-30Benadryl Ultratabs

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67751-166-01Benadryl Ultratabs2 in 1 POUCHTABLET, FILM COATED24
67751-166-01Benadryl Ultratabs1 in 1 CARTONTABLET, FILM COATED14
67751-166-02Benadryl Ultratabs1 in 1 CARTONTABLET, FILM COATED14
67751-166-02Benadryl Ultratabs4 in 1 POUCHTABLET, FILM COATED44

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67751-166BENADRYL ULTRATABS (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [NAVAJO MANUFACTURING COMPANY INC.]4Current NDC, Legacy NDC, 4 package rows20241004_76433e3c-142c-4704-8b2b-d602f008c377.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 22 of 190 · 3,793 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Vicks NyQuil Severe Cold and FluACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, AND PHENYLEPHRINE HYDROCHLORIDEThe Procter & Gamble Manufacturing Companyd1657403-b953-4db1-9a86-343e9e769a1a2026-06-22WarningsExact identifier
application number: M012
Vicks DayQuil and Vicks NyQuil Cold and FluACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, AND DOXYLAMINE SUCCINATEThe Procter & Gamble Manufacturing Company04dc3835-64be-d9e4-e063-6394a90a85992026-06-22WarningsExact identifier
application number: M012
Vicks DayQuil Kids COLD and COUGH plus FEVERACETAMINOPHEN, DEXTROMETHORPHAN HBRThe Procter & Gamble Manufacturing Company1a01b294-a5ee-ab35-e063-6394a90a4a1a2026-06-22WarningsExact identifier
application number: M012
Vicks NyQuil ALLERGYDOXYLAMINE SUCCINATEThe Procter & Gamble Manufacturing Company2f9b3bbb-4494-065d-e063-6294a90afcd22026-06-22WarningsExact identifier
application number: M012
Vicks NyQuil Kids ALLERGYDOXYLAMINE SUCCINATEThe Procter & Gamble Manufacturing Company2f9a6d65-f849-af0a-e063-6394a90ae4352026-06-22WarningsExact identifier
application number: M012
Allergy ReliefDIPHENHYDRAMINE HCLBIONPHARMA INC.3c1953a1-32e9-6c81-e063-6294a90a9fa22026-06-22WarningsExact identifier
application number: M012
Vicks NyQuil Kids COLD and COUGH plus FEVERACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATEThe Procter & Gamble Manufacturing Company1a01d4f7-37ed-bb92-e063-6294a90a208c2026-06-22WarningsExact identifier
application number: M012
Vicks DayQuil INTENSE FLUACETAMINOPHEN, DEXTROMETHORPHAN HBRThe Procter & Gamble Manufacturing Company326ed27d-cbfa-5513-e063-6394a90a41bf2026-06-22WarningsExact identifier
application number: M012
Vicks DayQuil Kids and Vicks NyQuil Kids COLD and COUGH plus FEVERACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATEThe Procter & Gamble Manufacturing Company2d430264-074d-fb22-e063-6294a90a57f62026-06-22WarningsExact identifier
application number: M012
DayQuil VapoCOOL SEVERE COLD and FLU plus CONGESTIONACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDE, AND GUAIFENESINThe Procter & Gamble Manufacturing Companyef6e8503-d268-291b-e053-2995a90aec8f2026-06-22WarningsExact identifier
application number: M012
Vicks DayQuil and Vicks NyQuil Severe Cold and FluACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, AND DOXYLAMINE SUCCINATEThe Procter & Gamble Manufacturing Company4147ff00-8e21-7335-e054-00144ff88e882026-06-22WarningsExact identifier
application number: M012
Allergy ReliefDIPHENHYDRAMINE HCLAMERISOURCE BERGEN51021c69-d92b-0504-e063-6294a90a94e72026-06-22WarningsExact identifier
application number: M012
Vicks NyQuil SINUS PAIN and HEADACHEACETAMINOPHEN, DOXYLAMINE SUCCINATEThe Procter & Gamble Manufacturing Company4c4ca296-ea6c-1f19-e063-6294a90a81612026-06-22WarningsExact identifier
application number: M012
Vicks DayQuil and Vicks NyQuil INTENSE FLUACETAMINOPHEN, DEXTROMETHORPHAN HBRThe Procter & Gamble Manufacturing Company32bea3dc-9889-22dd-e063-6394a90afa1b2026-06-22WarningsExact identifier
application number: M012
DAYTIME COLD AND FLUACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDECVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED59db2573-7ebb-4cf9-bfe3-428929bb4eeb2026-06-22WarningsExact identifier
application number: M012
Daytime Cold and FluACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDEBest Choice (Valu Merchandisers Company)bfec14d5-d9ce-4b9c-a803-3d01cb00b56c2026-06-22WarningsExact identifier
application number: M012
Sinus and Congestion Non-DrowsyPSEUDOEPHEDRINE HCLWal-Mart Stores Inccbdac7ad-3904-4a85-91a9-863f6f06503d2026-06-22WarningsExact identifier
application number: M012
Cold and Flu ReliefACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDEWinCo Foods, LLC5f1aaa8e-c65f-43b3-9850-c60c1663d78f2026-06-22WarningsExact identifier
application number: M012
DAY TIME INTENSE FLUACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDEMeijer, Inc.e5a64d5a-c1ff-453d-b0c1-fe265b9e2c8a2026-06-22WarningsExact identifier
application number: M012
NO DRIP NASALPHENYLEPHRINE HYDROCHLORIDECVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED7a866cdf-1c0c-403a-afc8-0e99e0ce81aa2026-06-22WarningsExact identifier
application number: M012

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1049632Benadryl 25 MG Oral TabletPSN76433e3c-142c-4704-8b2b-d602f008c3774
1049630diphenhydrAMINE HCl 25 MG Oral TabletPSN76433e3c-142c-4704-8b2b-d602f008c3774
1049632diphenhydramine hydrochloride 25 MG Oral Tablet [Benadryl]SBD76433e3c-142c-4704-8b2b-d602f008c3774
1049630diphenhydramine hydrochloride 25 MG Oral TabletSCD76433e3c-142c-4704-8b2b-d602f008c3774
1049632Benadryl 25 MG Oral TabletSY76433e3c-142c-4704-8b2b-d602f008c3774
1049632Benadryl Allergy Ultratab 25 MG Oral TabletSY76433e3c-142c-4704-8b2b-d602f008c3774

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
67751-166-01677510166011 POUCH in 1 CARTON (67751-166-01) / 2 TABLET, FILM COATED in 1 POUCH1 pouch2016-09-220000-00-00NoNoCurrent
67751-166-02677510166021 POUCH in 1 CARTON (67751-166-02) / 4 TABLET, FILM COATED in 1 POUCH1 pouch2016-09-220000-00-00NoNoCurrent