FDA.reportPublic FDA data

Ivy-Dry Super

Manufacturer
Ivy-Dry, Inc.
Effective date
2017-12-27
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 22:53:43

Label at a glance#

ProductIvy-Dry Super
Active ingredientBENZYL ALCOHOL, CAMPHOR (SYNTHETIC), MENTHOL
Label structure7 sections

Indications and uses

for the temporary relief of itching associated with insect bites and minor skin irritations

Dosage and administration

Apply to affected area not more than 3 times daily. Children under 6 years of age: do not use, ask a doctor. Severe reactions to Urushiol (the chemical released by the plant, which causes the irritation) can look like chemical burns and have a thick leathery appearance. Additional applications may be necessary. Test product on small patch of skin before applying to the entire body.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzyl Alcohol 10%

Camphor 0.5%

Menthol 0.25%

Purpose

OTC - PURPOSE SECTION

External Analgesic

Uses

INDICATIONS & USAGE SECTION


  • for the temporary relief of itching associated with insect bites and minor skin irritations

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • on face or genital areas
  • on areas of blistered or broken skin
  • with a compress after application

When using this product

OTC - WHEN USING SECTION

  • do not get into eyes
  • if contact occurs, flush eyes with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • symptoms last more than 7 days or clear up and occur again within a few days.

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a doctor before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION


  • Apply to affected area not more than 3 times daily.
  • Children under 6 years of age: do not use, ask a doctor.
  • Severe reactions to Urushiol (the chemical released by the plant, which causes the irritation) can look like chemical burns and have a thick leathery appearance. Additional applications may be necessary.
  • Test product on small patch of skin before applying to the entire body.

Other information

OTHER SAFETY INFORMATION

Store at room temperature

You may report a serious adverse reaction to Report Reaction, LLC PO Box 22 Plainsboro, NJ 08536-0222

Inactive Information

INACTIVE INGREDIENT SECTION

Water, Isopropanol, Zinc Acetate, Isoceteth-20, Zinc Lactate.

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sprays at any angle!


Ivy-Dry Super

Continuous Spray

TEMPORARY RELIEF OF PAIN AND ITCHING

External Analgesic

Manufactured for:
Ivy-Dry, Inc.
299-B Fairfield Avenue
Fairfield, NJ 07070
Made In Canada
©2012 Ivy-Dry, Inc.
Questions or Comments
www.ivydry.com

Ivy-Dry SuperIvy-Dry Super

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1302630benzyl alcohol 10 % / camphor 0.5 % / menthol 0.25 % Topical SprayPSN4
1302633IVY DRY SUPER 10 % / 0.5 % / 0.25 % Topical SprayPSN4
1302633benzyl alcohol 0.1 ML/ML / camphor 5 MG/ML / menthol 2.5 MG/ML Topical Spray [Ivy Dry Super Continuous Spray]SBD4
1302630benzyl alcohol 0.1 ML/ML / camphor 5 MG/ML / menthol 2.5 MG/ML Topical SpraySCD4
1302630benzyl alcohol 10 % / camphor 0.5 % / menthol 0.25 % Topical SpraySY4
1302633Ivy Dry Super Continuous Spray (benzyl alcohol 10 % / camphor 0.5 % / menthol 0.25 % ) Topical SpraySY4

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
BENZYL ALCOHOL Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49546-105-032022-01-28C16284748780-1d6a99b39-82cf-a426-e053-dadaa90af4c2Ivy-Dry Super

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49546-105-03Ivy-Dry Super89 mL in 1 CANISTERSPRAY894

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49546-105IVY-DRY SUPER (BENZYL ALCOHOL, CAMPHOR, MENTHOL) SPRAY [IVY-DRY, INC.]4Legacy NDC, 1 package rows20171227_22014fde-2648-4514-99c5-668481fa12c1.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BENZYL ALCOHOLACTIVE INGREDIENTLKG8494WBH3
CAMPHOR (SYNTHETIC)ACTIVE INGREDIENT5TJD82A1ET3
MENTHOLACTIVE INGREDIENTL7T10EIP3A3
BENZYL ALCOHOLACTIVE MOIETYLKG8494WBH3
CAMPHOR (SYNTHETIC)ACTIVE MOIETY5TJD82A1ET3
MENTHOLACTIVE MOIETYL7T10EIP3A3
ISOCETETH-20INACTIVE INGREDIENTO020065R7Z3
ISOPROPYL ALCOHOLINACTIVE INGREDIENTND2M4163023
WATERINACTIVE INGREDIENT059QF0KO0R3
ZINC ACETATEINACTIVE INGREDIENTFM5526K07A3
ZINC LACTATEINACTIVE INGREDIENT2GXR25858Y3

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49546-10549546-105-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302IACT
ZINC ACETATEFM5526K07AIACT
ISOCETETH-20O020065R7ZIACT
ZINC LACTATE2GXR25858YIACT
BENZYL ALCOHOLLKG8494WBHACTIB
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB
MENTHOLL7T10EIP3AACTIB

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 12 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ZINC ACETATEZINC ACETATEFM5526K07AINJECTION, POWDER, FOR SUSPENSION / SUBCUTANEOUS2.3 mgExact identifier — unii candidate
3 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302LOTION, AUGMENTED / TOPICAL2070 mgExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302TABLET, EXTENDED RELEASE / ORALNAExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302SOLUTION / TOPICAL40 %w/vExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302SPONGE / TOPICAL4 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302GEL / TOPICAL75 mgExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302GEL, METERED / TOPICAL525 mgExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302OIL / AURICULAR (OTIC)6 mgExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302OIL / TOPICAL72 mgExact identifier — unii candidate
9 equally ranked IID candidates
ZINC ACETATEZINC ACETATEFM5526K07AINJECTION / SUBCUTANEOUSNAExact identifier — unii candidate
3 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302SWAB / TOPICAL43.9 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
ZINC ACETATEZINC ACETATEFM5526K07ASWAB / TOPICALNAExact identifier — unii candidate
3 equally ranked IID candidates

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
6154b5de-86a7-9252-e053-2991aa0ad34522014fde-2648-4514-99c5-668481fa12c12017-12-27WarningsExact identifier
spl id: 6154b5de-86a7-9252-e053-2991aa0ad345
spl set id: 22014fde-2648-4514-99c5-668481fa12c1

Reported adverse events (FAERS/openFDA)#

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