Home NDC 69396-025 Anti-Itch Cream
Product NDC 69396-025
11-digit product format 693960025
Labeler code 69396
Product ID 69396-025_0df7f83e-5adb-ec48-e063-6294a90a198e
Type HUMAN OTC DRUG
Nonproprietary name Diphenhydramine hydrochloride 2%, zinc acetate 0.1%
Dosage form CREAM
Route TOPICAL
Labeler Trifecta Pharmaceuticals USA, LLC.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2016-12-29
Substance DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE
Active strength 2; .1 g/100g; g/100g
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 Anti-Itch Cream
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIPHENHYDRAMINE HYDROCHLORIDE 2 g/100g ZINC ACETATE .1 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination TC2D6JAD40 Internal UNII lookup FM5526K07A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1087026 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69396-025-05 Anti-Itch Cream 1 in 1 BOX CREAM 1 5 69396-025-05 Anti-Itch Cream 15 g in 1 TUBE CREAM 15 5 69396-025-15 Anti-Itch Cream 42 g in 1 TUBE CREAM 42 5 69396-025-15 Anti-Itch Cream 1 in 1 BOX CREAM 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69396-025 ANTI-ITCH CREAM (DIPHENHYDRAMINE HYDROCHLORIDE 2%, ZINC ACETATE 0.1%) CREAM [TRIFECTA PHARMACEUTICALS USA, LLC.] 5 Current NDC, Legacy NDC, 4 package rows 20240103_44d17651-a31b-64ca-e054-00144ff8d46c.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 149 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Bakers Best Maximum Strength Pain Relief LIDOCAINE HYDROCHLORIDE, MENTHOL Baker's Best Health Products, LLC 9d160ff1-9c23-4a5d-82b3-82c2e1e7d34d 2023-11-06 Warnings Exact identifier application number: M017 BAKERS BEST Pain Relief with Pure Hemp Seed Oil LIDOCAINE HYDROCHLORIDE, MENTHOL BAKER'S BEST HEALTH PRODUCTS, INC. ae54c234-bfe4-4a74-b293-db7efda7884b 2023-11-06 Warnings Exact identifier application number: M017 Arth RX Topical Analgesic METHYL NICOTINATE, CAPSAICIN HCD Sales a7b3b9b4-b1c4-4e51-8e3a-c84f64c75609 2023-11-06 Warnings Exact identifier application number: M017 BAKERS BEST Arthritis Pain Relief Cream with Hemp and Lavender HISTAMINE DIHYDROCHLORIDE BAKER'S BEST HEALTH PRODUCTS, INC. 03ec87c5-6669-4afb-8d9c-c8dc9907495d 2023-11-06 Warnings Exact identifier application number: M017 DOCTORS TOUCH Erase The Pain MENTHOL DOCTOR'S CHOICE MEDICAL, LLC fe9ce2c7-d6af-4dad-b6e6-5049a9e091b0 2023-11-06 Warnings Exact identifier application number: M017 RadiaGuard Advanced Radiation Relief LIDOCAINE HYDROCHLORIDE SMOOTH SIDE, INC 21205087-5a2e-41a5-be40-30cba2895408 2023-11-06 Warnings Exact identifier application number: M017 BLUE SPRING Foot and Leg Comfort MENTHOL ACA MANAGEMENT LLC 5f52218d-eea4-4640-b820-84c077ab98ba 2023-11-06 Warnings Exact identifier application number: M017 EMU THERAPY Red Hot Pepper Pain Relief Cream MENTHOL, CAPSAICIN ACA MANAGEMENT LLC 36293885-b2dd-4fba-9748-35a3c9e05078 2023-11-06 Warnings Exact identifier application number: M017 ROPANA Pain Relief Cream HISTAMINE DIHYDROCHLORIDE FUSION PAIN SOLUTIONS LLC e0342aa3-ca80-40b7-bec6-1b33c4db398b 2023-11-06 Warnings Exact identifier application number: M017 EMU THERAPY Cool Menthol Therapy Pain Relief Cream MENTHOL ACA MANAGEMENT LLC 16894346-3513-41b1-b09f-72d84edcc4ac 2023-11-06 Warnings Exact identifier application number: M017 SKINS DELAY Climax Control Lidocaine LIDOCAINE HYDROCHLORIDE SKINS SEXUAL HEALTH LIMITED 0db91010-12f7-4f20-b96c-432915720d5a 2023-11-06 Warnings Exact identifier application number: M017 POWERECT Lidocaine Male Delay LIDOCAINE HYDROCHLORIDE SKINS SEXUAL HEALTH LIMITED 42e0c40f-1efd-45ef-815d-53d193d720eb 2023-11-06 Warnings Exact identifier application number: M017 ARTHRO LIFE Instant Pain Relief Cream MENTHOL BIOBEST SERVICES LLC 66eb1a78-6861-4693-b68e-bd4a664fc075 2023-11-06 Warnings Exact identifier application number: M017 PARACTIN QuantumActiv Pain Relief Cream MENTHOL NHR SCIENCE CORP ae2f89cf-120c-4c6f-9e81-4560e6fa0373 2023-11-06 Warnings Exact identifier application number: M017 FISICO Arthrozene Pain Cream MENTHOL FISICO INC. d02c4349-78dd-4672-9582-50124ea9f1e1 2023-11-06 Warnings Exact identifier application number: M017 BRONSON SOOTHE Pain Relief CAPSAICIN BRONSON NUTRITIONALS, LLC cedf8f43-b9a3-4a06-b3a1-cf82668541f8 2023-11-06 Warnings Exact identifier application number: M017 INTIMALE Benzocaine Delay Gel BENZOCAINE SKINS SEXUAL HEALTH LIMITED b845bfd5-ab73-495f-97ef-e959bc6311d9 2023-11-06 Warnings Exact identifier application number: M017 RAPID PAIN-RELIEF TOPICAL LIDOCAINE HYDROCHLORIDE, MENTHOL NORDIC HEALTHY LIVING INC. a06d6aca-9aa2-4bbe-bf77-4c85f1dd7870 2023-11-06 Warnings Exact identifier application number: M017 PURE PERSONAL All Natural Pain Relief Cream MENTHOL PURE PERSONAL CARE, LLC 8f3fb1d0-d238-4b4c-9816-7e335258d71d 2023-11-06 Warnings Exact identifier application number: M017 DIRT Pain Relieving Gel MENTHOL PURIVITAE, LLC 89c80a8f-227d-4ec0-9327-683892e73b6a 2023-11-06 Warnings Exact identifier application number: M017
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69396-025-05 69396002505 1 TUBE in 1 BOX (69396-025-05) / 15 g in 1 TUBE 1 tube 2016-12-29 0000-00-00 No No Current 69396-025-15 69396002515 1 TUBE in 1 BOX (69396-025-15) / 42 g in 1 TUBE 1 tube 2020-02-11 0000-00-00 No No Current