FDA.reportPublic FDA data

ChigaRid

Manufacturer
Colgin Inc
Effective date
2024-10-15
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 20:52:25

Label at a glance#

ProductChigaRid
Active ingredientCAMPHOR (SYNTHETIC), PHENOL, MENTHOL
Label structure7 sections

Indications and uses

For the temporary relief of pain and itching associated with insect bites.

Dosage and administration

Clean and dry affected area. Apply using Chigarid applicator cap. Adults and children 2 years and older: apply to affected area 3 to 4 times daily. Children under 2 years of age: consult a physician or doctor.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Camphor 2.6%, Phenol 1.5%, Menthol 0.1%

OTC - PURPOSE SECTION

External Analgesic

USES:

INDICATIONS & USAGE SECTION

For the temporary relief of pain and itching associated with insect bites.

WARNINGS:

WARNINGS SECTION

Avoid contact with the eyes. Do not apply over large areas of the body. For external use only. Highly flammable.

Keep out of reach of children. 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

STOP USE AND ASK A DOCTOR IF

OTC - STOP USE SECTION

condition worsens or if symptoms persist for more than 7 days or clear up and return within a few days.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Clean and dry affected area. Apply using Chigarid applicator cap. Adults and children 2 years and older: apply to affected area 3 to 4 times daily. Children under 2 years of age: consult a physician or doctor.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Anisole, NQ Cotton, Methyl Ethyl Ketone, Methyl Isobutyl Ketone, Castor oil, Dibutyl Phthalate, Isopropyl Alcohol, Eucalyptus oil

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47047-000147047-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ANISOLEB3W693GAZHIACT
METHYL ETHYL KETONE6PT9KLV9IOIACT
METHYL ISOBUTYL KETONEU5T7B88CNPIACT
CASTOR OILD5340Y2I9GIACT
DIBUTYL PHTHALATE2286E5R2KEIACT
ISOPROPYL ALCOHOLND2M416302IACT
EUCALYPTUS OIL2R04ONI662IACT
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB
PHENOL339NCG44TVACTIB
MENTHOLL7T10EIP3AACTIB

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
2483acec-42ed-617a-e063-6294a90a4963dfed19af-75d5-4daa-b61f-e7e3bf680fb62024-10-15WarningsExact identifier
spl id: 2483acec-42ed-617a-e063-6294a90a4963
spl set id: dfed19af-75d5-4daa-b61f-e7e3bf680fb6

Reported adverse events (FAERS/openFDA)#

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