FDA.reportPublic FDA data

ProCure DryDrox

Manufacturer
Twin Med LLC
Effective date
2025-09-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:13:40

Label at a glance#

ProductProCure DryDrox
Active ingredientALUMINUM HYDROXIDE
Label structure7 sections

Indications and uses

Uses Dries the oozing and weeping of poison ivy, oak and sumac

Dosage and administration

Directions Apply as needed Children under 6 months of age: ask a doctor

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Hydroxide Gel 2%

Purpose

OTC - PURPOSE SECTION

Skin Protectant

Uses

INDICATIONS & USAGE SECTION

Uses

  • Dries the oozing and weeping of poison ivy, oak and sumac

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

  • Apply as needed
  • Children under 6 months of age: ask a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Calcium Carbonate, Cholecalciferol, Citric Acid, Ethylhexylglycerin, Glyceryl Monostearate, Glyceryl Stearate/ PEG-100 Stearate, Lanolin, Magnesium Hydroxide, Petrolatum, Phenoxyethanol, Propylene Glycol, Retinyl Palmitate, Sodium Chloride, Sodium Laureth Sulfate,Stearyl Alcohol, Water, Zea Mays Corn Oil, Zinc Chloride

Warnings

WARNINGS SECTION

Warnings

For external use only

When using this product

OTC - WHEN USING SECTION

When using this productdo not get into the eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • Condition worsens
  • Symptoms last more than 7 days or clear up and occur again within a few days

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.In case of accidental ingestion contact a physician or Poison Control Center right away.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PCMG35 ImagePCMG35 Image

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
60c52429-fcef-eb54-2387-43bc9e4f296bProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55681-031-04ProCure DryDrox106 g in 1 TUBEOINTMENT1061

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55681-03155681-031-04

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
ZEA MAYS (CORN) OIL8470G57WFMIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
LANOLIN7EV65EAW6HIACT
MAGNESIUM HYDROXIDENBZ3QY004SIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
CALCIUM CARBONATEH0G9379FGKIACT
CHOLECALCIFEROL1C6V77QF41IACT
CITRIC ACID2968PHW8QPIACT
GLYCERYL STEARATE/PEG-100 STEARATERD25J5V947IACT
PETROLATUM4T6H12BN9UIACT
PHENOXYETHANOLHIE492ZZ3TIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
RETINYL PALMITATE1D1K0N0VVCIACT
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
STEARYL ALCOHOL2KR89I4H1YIACT
WATER059QF0KO0RIACT
ZINC CHLORIDE86Q357L16BIACT
ALUMINUM HYDROXIDE5QB0T2IUN0ACTIB

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ProCure DryDroxALUMINUM HYDROXIDE GEL 2%Twin Med LLC3ab4efb6-bd31-2583-e063-6294a90a415b2025-09-15WarningsExact identifier
ndc (package): 55681-031-04
ndc (product): 55681-031
ndc11 (package): 55681003104
spl id: 3ab4efb6-bd31-2583-e063-6294a90a415b
spl set id: 3ab4efb6-bd31-2583-e063-6294a90a415b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.