Poison Ivy Wash

Manufacturer
Chain Drug Market Association | Pharma Nobis, LLC
Effective date
2023-12-20
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:05:10

Label at a glance#

ProductPoison Ivy Wash
Active ingredientPRAMOXINE HYDROCHLORIDE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Pramoxine HCl 1%

OTC - PURPOSE SECTION

External Analgesic

INDICATIONS & USAGE SECTION

For temporary relief of pain and itching associated with poison ivy, poison oak, and poison sumac.

WARNINGS SECTION

For external use only.

When using this product:

Avoid Contact with eyes.

Do not leave on skin longer than 3 minutes

Rinse thoroughly after application

OTC - WHEN USING SECTION

When using this product avoid contact with the eyes. Do not leave on skin longer than 3 minutes. Rinse thoroughly after application.

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if condition worses, or if symptoms persist for more than 7 days or clear up and occur again within a few days.

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 years of age and older: wet the affected area, apply product to affected skin and surrounding area. work foam into lather and rub for up to 3 minutes if needed. do not leave on skin for longer than 3 minutes. Thoroughly rinse product form all areas. Apply to affected are not more than 3 to 4 times daily.

INACTIVE INGREDIENT SECTION

Water

ammonium lauryl sulfare

distearyl phtalic acid amide

glycol distereate

cocamide MIPA

Propylene glycol

Diazolidyn Urea

Methylparaben
Propylparaben

Glycerin

Jojoba esters

disodium edta

sodium hydroxide

nonoxynol-9

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a poison control center immediately.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

washwash

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1247251pramoxine HCl 1 % Medicated Liquid SoapPSN4
1247251pramoxine hydrochloride 10 MG/ML Medicated Liquid SoapSCD4
1247251pramoxine hydrochloride 1 % Medicated Liquid SoapSY4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
777d68c6-a5ab-e06c-d314-677b0b9af0c8Product name220240508
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
63868-877-06Poison Ivy Wash177 mL in 1 CONTAINERLOTION1774

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63868-877POISON IVY WASH (PRAMOXINE HCL) LOTION [CHAIN DRUG MARKET ASSOCIATION]4Current NDC, Legacy NDC, 1 package rows20231221_873a546b-90ae-50cb-e053-2a91aa0adbfb.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63868-877-06ML - Milliliter63868-877d96a5ad4-0004-4c8c-9157-28f2e46b278c12022-10-06

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63868-87763868-877-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

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
Poison Ivy WashPRAMOXINE HCLChain Drug Market Association873a546b-90ae-50cb-e053-2a91aa0adbfb2023-12-20WarningsExact identifier
ndc (package): 63868-877-06
ndc (product): 63868-877
ndc11 (package): 63868087706
spl id: 0cf4cb65-adda-e3ca-e063-6294a90a3e30
spl set id: 873a546b-90ae-50cb-e053-2a91aa0adbfb

Reported adverse events (FAERS/openFDA)#

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