Home NDC 10157-2125 Ivarest Poison Ivy Removal and Itch Relief
Product NDC 10157-2125
11-digit product format 101572125
Labeler code 10157
Product ID 10157-2125_61e42ae1-bdd5-43fb-a98e-3d28f0651074
Type HUMAN OTC DRUG
Nonproprietary name PRAMOXINE HYDROCHLORIDE
Dosage form LIQUID
Route TOPICAL
Labeler Blistex Inc.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-02-01
Substance PRAMOXINE HYDROCHLORIDE
Active strength 1 g/100mL
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 Ivarest Poison Ivy Removal and Itch Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PRAMOXINE HYDROCHLORIDE 1 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 88AYB867L5 Internal UNII 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 10157-2125-1 Ivarest Poison Ivy Removal and Itch Relief 1 in 1 CARTON LIQUID 1 1 10157-2125-1 Ivarest Poison Ivy Removal and Itch Relief 30 in 1 JAR LIQUID 30 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10157-2125 IVAREST POISON IVY REMOVAL AND ITCH RELIEF (PRAMOXINE HYDROCHLORIDE) LIQUID [BLISTEX INC.] 1 Current NDC, 2 package rows 20250501_dedbf5d9-0f86-4f32-8321-da86c9838c0a.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 29 of 152 · 3,029 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Walgreens Burn Pad BURN PAD Walgreens 3f8d7624-cf1e-1992-e063-6294a90a3806 2026-03-17 Boxed warning, Warnings Exact identifier application number: M017 Hydrocortisone HYDROCORTISONE Mericon Industries 8f351b04-8f6d-4353-9100-13a8a80d656a 2026-03-17 Warnings Exact identifier application number: M017 Shoe Pain Relief LIDOCAINE HCI 4% Sole Amie 0f2ccd5f-b9f4-40fc-b82f-173b0f19bf40 2026-03-16 Warnings Exact identifier application number: M017 CVS Muscle Balm MENTHOL, CAMPHOR CVS Health 42796fc4-03be-3b02-e063-6394a90af2ab 2026-03-16 Warnings Exact identifier application number: M017 Crane Safety Hydrocortisone HYDROCORTISONE Crane Safety LLC 96d9527d-9bf7-ce82-e053-2995a90aff0c 2026-03-16 Warnings Exact identifier application number: M017 CVS Health Pain Relief Foot MENTHOL, UNSPECIFIED FORM NATURAL ESSENTIALS, INC. 0f646876-69d0-49db-ade2-2b3eb26dd399 2026-03-16 Warnings Exact identifier application number: M017 Walgreens Cold Therapy Pain Relief Foot Cream MENTHOL Walgreen Co. 3bc8ece3-d555-3efb-e063-6394a90a1981 2026-03-16 Warnings Exact identifier application number: M017 RICHTOFIT RAPID ACTIVE LEG AND FOOT MENTHOL RICHTOFIT LIMITED LIABILITY COMPANY 4c357696-ca96-e6ad-e063-6294a90aaadb 2026-03-16 Warnings Exact identifier application number: M017 Xpect Stopain Clinical MENTHOL Cintas Corporation 348e6062-b31e-435e-a153-6aa868b50efa 2026-03-13 Warnings Exact identifier application number: M017 DGH GREASELESS MUSCLE RUB ANALGESIC MENTHOL, UNSPECIFIED FORM AND METHYL SALICYLATE DOLLAR GENERAL 225abfe0-ec72-4667-96b2-7657e989672b 2026-03-13 Warnings Exact identifier application number: M017 CVS Professional Pain Relief MENTHOL CVS Pharmacy 48836a5b-0baa-b7ee-e063-6294a90ac12b 2026-03-13 Warnings Exact identifier application number: M017 Keeps Climax Delay LIDOCAINE HYDROCHLORIDE Cosco International, Inc. 3bfd3173-2dac-40a9-aec3-982b1d47d8fa 2026-03-12 Warnings Exact identifier application number: M017 NanoX Pain Relieving MENTHOL, METHYL SALICYLATE MG Science Technologies LLC 4cc38927-8a8c-2df3-e063-6294a90aa0c1 2026-03-12 Warnings Exact identifier application number: M017 Hand Sanitizer ALCOHOL ProStat First Aid 4cd4c51c-88bb-3797-e063-6294a90a8f70 2026-03-12 Warnings Exact identifier application number: M017 CVS Lidocaine Pain Relief LIDOCAINE HYDROCHLORIDE, MENTHOL CVS Pharmacy 48c045ae-56b5-62c2-e063-6394a90aaf44 2026-03-12 Warnings Exact identifier application number: M017 Hydrocortisone 1% HYDROCORTISONE ProStat First Aid 4cd62cba-075a-7448-e063-6394a90ab48d 2026-03-12 Warnings Exact identifier application number: M017 Medicated Pain Relief Patch CAMPHOR, MENTHOL, METHYL SALICYLATE Kroger Company 47cc4b05-a937-4624-bf41-85b8bd7c049e 2026-03-12 Warnings Exact identifier application number: M017 Lidocaine HCL LIDOCAINE HCL Matthias Therapeutics, LLC 4cdb27b5-9178-0328-e063-6394a90a50b5 2026-03-12 Warnings Exact identifier application number: M017 RICHTOFIT RAPID ACTIVE ARTHRITIS MENTHOL AND CAMPHOR RICHTOFIT LIMITED LIABILITY COMPANY 4b1cdab1-3e50-4ec3-e063-6394a90af75e 2026-03-12 Warnings Exact identifier application number: M017 5Kind DMSO 4 Lidocaine HCl Pain Relieving LIDOCAINE HYDROCHLORIDE, MENTHOL 5KIND TRADING LTD 67d8d045-7fa0-46c2-8072-645d8823903b 2026-03-11 Warnings Exact identifier application number: M017
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 10157-2125-1 10157212501 1 JAR in 1 CARTON (10157-2125-1) / 30 APPLICATOR in 1 JAR / 2 mL in 1 APPLICATOR 1 jar 2025-02-01 No No Current