FDA.reportPublic FDA data

Chiggerex 2X Medicated

Manufacturer
Product Quest Mfg
Effective date
2017-10-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:52:37

Label at a glance#

ProductChiggerex 2X Medicated
Active ingredientBenzocaine
Label structure6 sections

Indications and uses

Temporarily relieves pain and itching due tochigger bites, red bug bites, ticks, mosquito bites

Dosage and administration

• adults and children 12 years of age and older: apply to affected area, not more than 3 to 4 times daily. Children under 2 years of age: consult a doctor

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient                             Purpose

Benzocaine  10.0%                         Pain Relief

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves pain and itching due tochigger bites, red bug bites, ticks, mosquito bites

WarningsFor external use only

WARNINGS SECTION

When using this product avoid contact with the eyes

Stop use and ask a doctor if rash occurs
• condition worsens
• symptoms last more than 7 days or clear up and occur again within a few days

Keep out of reach of children. If swallowed, contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

• adults and children 12 years of age and older: apply to affected area, not more than 3 to 4 times daily. Children under 2 years of age: consult a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water
PEG-2 Stearate SE, PEG-2 Stearate
Olea Europaea (Olive) Fruit Extract
Aloe Barbadensis Leaf Juice
Methylparaben
Diazolidinyl Urea
Mentha Piperita (Peppermint) Oil
Eugenia Caryophyllus (Clove) Flower Oil
Propylparaben
Chamomilla Recutita (Matricaria) Flower Extract
PEG-8 Dimethicone, Zea Mays (Corn) Oil, Propylene Glycol, Octyldodecanol, Tocopheryl
Acetate, Ascorbic Acid, Retinyl Palmitate, Pyridoxine HCl, Cholecalciferol, Sodium
Propoxyhydroxypropyl Thiosulfate Silica
Fragrance
Disodium EDTA
Camphor

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
197395benzocaine 10 % Topical OintmentPSN1
1946727Chiggerex 10 % Topical OintmentPSN1
1946727benzocaine 0.1 MG/MG Topical Ointment [Chiggerex]SBD1
197395benzocaine 0.1 MG/MG Topical OintmentSCD1
197395benzocaine 10 % Topical OintmentSY1
1946727Chiggerex 0.1 MG/MG Topical OintmentSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
BENZOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130727510003795GTIN-13: 0727510003795
EAN-13: 0727510003795
GTIN-12: 727510003795
UPC-A: 727510003795
GTIN storage (14 digits): 00727510003795		label.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
59361619-24d9-b610-eca6-5a7f25ed5e03Product name520240909
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
5e18e798-5614-cf5c-0185-38b1cb77a093Product name220160822
60c52429-fcef-eb54-2387-43bc9e4f296bProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64048-1111-12020-01-31C16284748780-19d75b9d0-60b2-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64048-1111-1Chiggerex 2X Medicated50 g in 1 TUBEOINTMENT501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64048-1111CHIGGEREX 2X MEDICATED (BENZOCAINE 10.0%) OINTMENT [PRODUCT QUEST MFG]1Legacy NDC, 1 package rows20171004_646bef19-f1f8-4f3c-a2b7-876f7b84ff8c.zip

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64048-111164048-1111-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
BenzocaineU3RSY48JW5ACTIB
Water059QF0KO0RIACT
PEG-2 STEARATE94YQ11Y95FIACT
BLACK OLIVE2M6QWV94OCIACT
ALOE VERA LEAFZY81Z83H0XIACT
MethylparabenA2I8C7HI9TIACT
Diazolidinyl UreaH5RIZ3MPW4IACT
PEPPERMINT OILAV092KU4JHIACT
CLOVE OIL578389D6D0IACT
PropylparabenZ8IX2SC1OHIACT
CHAMOMILEFGL3685T2XIACT
PEG-8 DIMETHICONEGIA7T764ODIACT
CORN OIL8470G57WFMIACT
Propylene Glycol6DC9Q167V3IACT
Octyldodecanol461N1O614YIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
Ascorbic AcidPQ6CK8PD0RIACT
VITAMIN A PALMITATE1D1K0N0VVCIACT
PYRIDOXINE HYDROCHLORIDE68Y4CF58BVIACT
Cholecalciferol1C6V77QF41IACT
SODIUM PROPOXYHYDROXYPROPYL THIOSULFATE SILICA208G222332IACT
EDETATE DISODIUM7FLD91C86KIACT
CAMPHOR (SYNTHETIC)5TJD82A1ETIACT

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
8243fe09-590f-40fd-8ff7-cb266e80e924646bef19-f1f8-4f3c-a2b7-876f7b84ff8c2017-10-04WarningsExact identifier
spl id: 8243fe09-590f-40fd-8ff7-cb266e80e924
spl set id: 646bef19-f1f8-4f3c-a2b7-876f7b84ff8c

Reported adverse events (FAERS/openFDA)#

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