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 32 of 152 · 3,029 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Walgreens Pain Relieving Patch MENTHOL, CAMPHOR, METHYL SALICYLATE Walgreen Co. 4223c74a-12fb-51a3-e063-6294a90a0deb 2026-02-25 Warnings Exact identifier application number: M017 Advanced Pain Relief Roll-On Gel With 5% Natural Menthol MENTHOL Allure Labs 4bad597f-acb2-a122-e063-6394a90a9fcf 2026-02-25 Warnings Exact identifier application number: M017 Maximum Strength 4% Lidocaine Patch Good Neighbor Pharmacy LIDOCAINE InterMed Laboratories Private Limited 4bade8a9-43bd-b649-e063-6294a90a81da 2026-02-25 Warnings Exact identifier application number: M017 dermaFIT Muscle Retention Cream Strength MENTHOL EX Healthcare Inc. 4620c41a-2187-00f5-e063-6394a90a613c 2026-02-23 Warnings Exact identifier application number: M017 dermaFIT Muscle Retention Cream Sculpt MENTHOL EX Healthcare Inc. 4620d4ca-42e4-eeae-e063-6394a90a5c84 2026-02-23 Warnings Exact identifier application number: M017 dermaFIT Muscle Retention Cream Extra Strength MENTHOL EX Healthcare Inc. 4620ca7a-afe6-d063-e063-6394a90ab5db 2026-02-23 Warnings Exact identifier application number: M017 Hydrocortisone HYDROCORTISONE Sportpharm LLC 9578b39e-3df7-4d75-abd7-f1d5524545e5 2026-02-23 Warnings Exact identifier application number: M017 0.5% LIDOCAINE BURN RELIEF LIDOCAINE HYDROCHLORIDE Nantong Health & Beyond Hygienic Products Inc. cf723c7b-495d-4bae-942c-561cf28af2d3 2026-02-21 Warnings Exact identifier application number: M017 Swiftalyn Numbing Cream MENTHOL 1% GENUINE INNOVATION LTD 4b2ebff2-2f50-e54b-e063-6294a90aaccb 2026-02-19 Warnings Exact identifier application number: M017 Equate Cold Therapy Pain Relieving MENTHOL Walmart Inc 46a3c9e9-5cd3-4bc4-e063-6394a90a7178 2026-02-19 Warnings Exact identifier application number: M017 Itch Relief DIPHENHYDRAMINE HCL, ZINC ACETATE Meijer, Inc. e11390ec-99a3-4ff1-a3c8-ca909f4f67b5 2026-02-19 Warnings, Adverse reactions Exact identifier application number: M017 Aloe Vera Gel LIDOCAINE HCL, MENTHOL Meijer, Inc. d0cc06c1-c0d5-42f0-82cd-8b704cbe1f46 2026-02-19 Warnings, Adverse reactions Exact identifier application number: M017 MENTHOL, CAMPHOR MENTHOL, CAMPHOR CHEMCO CORPORATION 4b1a0e6f-aa68-421c-e063-6294a90a426e 2026-02-18 Warnings Exact identifier application number: M017 Veiurkiu External Analgesic Cream LIDOCAINE BLOOMWELL GARDENS LLC 40ec5e6f-13dc-de04-e063-6294a90af5d5 2026-02-18 Warnings Exact identifier application number: M017 External Analgesic Cream with Menthol 5% MENTHOL 5% BLOOMWELL GARDENS LLC 402faa27-5305-c73d-e063-6394a90a36f2 2026-02-18 Warnings Exact identifier application number: M017 PAINGEL MENTHOL, METHYL SALICYLATE NACOR BUSINESS GROUP LLC 4b1d55e2-cf83-ffbd-e063-6294a90ad52f 2026-02-18 Warnings Exact identifier application number: M017 Alocane Anti-Itch HYDROCORTISONE 1% Quest Products, LLC 45252043-d41a-3cdd-e063-6394a90aa9e5 2026-02-18 Warnings Exact identifier application number: M017 Hydrocortisone HYDROCORTISONE Medrock Pharmacy LLC 43e00e17-1a48-43db-9589-834568917bbf 2026-02-17 Warnings Exact identifier application number: M017 Tylenol Precise Cooling Pain Relieving LIDOCAINE, MENTHOL Kenvue Brands LLC fc0a3404-b174-3952-e053-6294a90a1e02 2026-02-16 Warnings Exact identifier application number: M017 Aloe Vera Gel LIDOCAINE HCL Valu Merchandisers Company 87ee2b4f-d640-4cec-9f48-1d8aa54434e9 2026-02-16 Warnings, Adverse reactions 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