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

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
IngredientStrength
PRAMOXINE HYDROCHLORIDE1 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii88AYB867L5

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
58f3f9b7-3b9b-a9c1-1c9f-18ac777192b8Product name120140508
a7051cba-790b-a699-81f8-dbbbdbd9b5acProduct name120140508
da108d9e-edc8-17a3-8c28-3251c6a8acccProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10157-2125-1Ivarest Poison Ivy Removal and Itch Relief1 in 1 CARTONLIQUID11
10157-2125-1Ivarest Poison Ivy Removal and Itch Relief30 in 1 JARLIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10157-2125IVAREST POISON IVY REMOVAL AND ITCH RELIEF (PRAMOXINE HYDROCHLORIDE) LIQUID [BLISTEX INC.]1Current NDC, 2 package rows20250501_dedbf5d9-0f86-4f32-8321-da86c9838c0a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
10157-2125-1101572125011 JAR in 1 CARTON (10157-2125-1) / 30 APPLICATOR in 1 JAR / 2 mL in 1 APPLICATOR1 jar2025-02-01NoNoCurrent