FDA.reportPublic FDA data

Benadryl Extra Strength Itch Relief

Product NDC
69968-0459
11-digit product format
699680459
Labeler code
69968
Product ID
69968-0459_399004db-8df3-c030-e063-6294a90a260b
Type
HUMAN OTC DRUG
Nonproprietary name
DIPHENHYDRAMINE HYDROCHLORIDE and Zinc Acetate
Dosage form
SOLUTION
Route
TOPICAL
Labeler
Kenvue Brands LLC
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-06-01
Substance
ZINC ACETATE; DIPHENHYDRAMINE HYDROCHLORIDE
Active strength
1; 20 mg/mL; mg/mL
Pharmacologic classes
Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], 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 Extra Strength Itch Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZINC ACETATE1 mg/mL
DIPHENHYDRAMINE HYDROCHLORIDE20 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
FM5526K07AInternal UNII lookup
TC2D6JAD40Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1294589Internal RxNorm lookup
1294591Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
309d9be0-e367-429a-a1fa-ab7855477c8aAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
77dc03a4-fbfc-e6a3-fe95-285bbae40d75Product name220250814
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0e2e0f88-b076-afe1-4bdd-32bca4375becProduct name320250127
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508
3e48c9c4-918d-5d23-2f0b-d2398b06be54Product name120140508
865c72dd-0d94-daac-f728-ddd4ded2a79eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69968-0459-1Benadryl Extra Strength Itch Relief1 in 1 CARTONSOLUTION18
69968-0459-1Benadryl Extra Strength Itch Relief14 mL in 1 APPLICATORSOLUTION148

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69968-0459-1ML - Milliliter69968-04599fdb0baa-a35e-4a36-8cfc-37a065d225af12022-06-06

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69968-0459BENADRYL EXTRA STRENGTH ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE) SOLUTION [KENVUE BRANDS LLC]7Current NDC, Legacy NDC, 2 package rows20241103_309d9be0-e367-429a-a1fa-ab7855477c8a.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 26 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Dr SabharwalsLIDOCAINE 4% GEL PATCHDr. Sabharwal's Wound Care102399b6-5be9-ee5e-e063-6394a90a31982026-04-02WarningsExact identifier
application number: M017
TATTOO NUMBX NUMBING PAIN RELIEVINGLIDOCAINE HYDROCHLORIDEScyberco Ltdac8eac04-ed5b-4c8e-9f9b-54d160b746062026-04-02WarningsExact identifier
application number: M017
FifthPulse HydrocortisoneHYDROCORTISONEWeCare Products LLCf1fcb045-4a15-431b-9617-67eae9f87fbd2026-04-02WarningsExact identifier
application number: M017
ANIXIKE CreamMENTHOL 5% CREAMJiangxi Yudexi Pharmaceutical Co., LTD4e8510e6-c0c7-bf6b-e063-6294a90a3b002026-04-02WarningsExact identifier
application number: M017
RAPID RELIEF0.025% CAPSAICIN PAIN PATCH835694ed549e8-0062-fb03-e063-6294a90aac652026-04-02WarningsExact identifier
application number: M017
Itch ReliefDIPHENHYDRAMINE HCL AND ZINC ACETATECVS Pharmacy7e921988-ec66-38dc-e053-2a91aa0a73462026-04-01WarningsExact identifier
application number: M017
The Best Numbing CreamTBNCThe Best Numbing Cream LLC4ca3923b-f586-0aaf-e063-6294a90a16c12026-03-31WarningsExact identifier
application number: M017
ChapStick Classic MedicatedEXTERNAL ANALGESIC AND SKIN PROTECTANT LIP BALMSuave Brands Co., LLC42798a6c-2d7e-80f6-e063-6294a90a105f2026-03-31WarningsExact identifier
application number: M017
Roll-On Pain Relief LiquidLIDOCAINE HCLHyVee Inc4da6f6fb-b182-360f-e063-6294a90abdf32026-03-31WarningsExact identifier
application number: M017
Hand SanitizerALCOHOLProStat First Aid4e54aecb-190f-3866-e063-6294a90a810a2026-03-31WarningsExact identifier
application number: M017
Burn MistLIDOCAINE HYDROCHLORIDEWater-Jel Technologiesc53ab9dd-351a-400b-b873-4f396e0af54d2026-03-31WarningsExact identifier
application number: M017
Satohap Lidocaine Hydrochloride 4 Percent Pain RelievingLIDOCAINE HYDROCHLORIDESato Pharmaceutical Co., Ltd.f7faddb2-5153-4fdd-a5ef-778182cef4602026-03-31WarningsExact identifier
application number: M017
ZENOL COOLMETHYL SALICYLATE, L-MENTHOLBA TRADE INC4e5c45f4-88ce-3a13-e063-6394a90a2a092026-03-31WarningsExact identifier
application number: M017
Eagle Brand Medicated Roll On RefreshCAMPHOR, MENTHOLBorden Company (Private) Limited091451fb-e30a-0012-e063-6394a90a3ba82026-03-31WarningsExact identifier
application number: M017
Icy Hot Revive and Recovery Pain Relief No- Mess Roll On Refreshing Lime and MintMENTHOLChattem, Inc.b16ba9c2-23bf-4fdf-b44b-7abb9fec19112026-03-31WarningsExact identifier
application number: M017
DR.PABU NUMBINGLIDOCAINE 5% NUMBINGJiangxi Yudexi Pharmaceutical Co., LTD4e3a3c6c-4821-76ea-e063-6294a90a8f962026-03-30WarningsExact identifier
application number: M017
Doctor Jiao Antifungal CreamMICONAZOLE NITRATEJiangxi Haiwei Pharmaceutical Co., Ltd.4e3b231e-0642-bf63-e063-6394a90a905b2026-03-30WarningsExact identifier
application number: M017
CVS Muscle Balm and Roll-OnCAMPHOR, MENTHOLCVS Pharmacy4e40025a-070a-508e-e063-6394a90af5d72026-03-30WarningsExact identifier
application number: M017
REGENECARE HALIDOCAINE HCLMPM Medical LLCc3eec066-38e8-4617-b34d-2f72ffb7a3242026-03-30WarningsExact identifier
application number: M017
Softlips Naturals Medicated Matcha HoneyCAMPHOR, MENTHOLThe Mentholatum Company4e03a721-73f3-b2f2-e063-6394a90a44e62026-03-27WarningsExact identifier
application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1294591Benadryl 2 % / 0.1 % Topical SolutionPSN309d9be0-e367-429a-a1fa-ab7855477c8a8
1294589diphenhydrAMINE HCl 2 % / zinc acetate 0.1 % Topical SolutionPSN309d9be0-e367-429a-a1fa-ab7855477c8a8
1294591diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical Solution [Benadryl Itch Stopping]SBD309d9be0-e367-429a-a1fa-ab7855477c8a8
1294589diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical SolutionSCD309d9be0-e367-429a-a1fa-ab7855477c8a8
1294591Benadryl Extra Strength (diphenhydramine hydrochloride 2 % / zinc acetate 0.1 % ) Topical SolutionSY309d9be0-e367-429a-a1fa-ab7855477c8a8
1294591Benadryl Extra Strength Itch Relief Stick (diphenhydramine hydrochloride 2 % / zinc acetate 0.1 % ) Topical SolutionSY309d9be0-e367-429a-a1fa-ab7855477c8a8
1294589diphenhydramine hydrochloride 2 % / zinc acetate 0.1 % Topical SolutionSY309d9be0-e367-429a-a1fa-ab7855477c8a8

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69968-0459-1699680459011 APPLICATOR in 1 CARTON (69968-0459-1) / 14 mL in 1 APPLICATOR1 applicator2019-06-010000-00-00NoNoCurrent