Chigger Relief by Evora Worldwide / Inspec Solution Drug Facts

Chigger Relief by

Drug Labeling and Warnings

Chigger Relief by is a Otc medication manufactured, distributed, or labeled by Evora Worldwide, Inspec Solution. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CHIGGER RELIEF EVORA LABS- benzocaine 10% ointment 
Evora Worldwide

----------

Drug Facts

Active ingredient                               Purpose

Benzocaine 10%                                 Pain Relief

Uses

Temporary releif of pain and itching due to

• chigger bites
• red bug bites
• ticks
• mosquito bites

WarningsFor external use only.

When using this product avoid contact with eyes.

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

Keep out of reach of children

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

Directions

Adults and children 2 years of age and older: apply to affected arenot more than 3 to 4 times daily.

Children under 2 years of age: ask a doctor.

Inactive ingredients

WATER
PEG-2 STEARATE
OLEA EUROPAEA (OLIV) FRUIT EXTRACT
ALOE BARBADENSIS LEAF EXTRACT
METHYLPARABEN
DIAZOLIDINYL UREA
PEPPERMINT OIL
EUGENIA CARYOPFYLLUS (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

QUESTIONS?

1-888-793-8450

CHIGGER RELIEF  EVORA LABS
benzocaine 10% ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77375-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	10 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PEG-2 STEARATE (UNII: 94YQ11Y95F)
BLACK OLIVE (UNII: 2M6QWV94OC)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
METHYLPARABEN (UNII: A2I8C7HI9T)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
PEPPERMINT OIL (UNII: AV092KU4JH)
CLOVE OIL (UNII: 578389D6D0)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
CHAMOMILE (UNII: FGL3685T2X)
PEG-8 DIMETHICONE (UNII: GIA7T764OD)
CORN OIL (UNII: 8470G57WFM)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
OCTYLDODECANOL (UNII: 461N1O614Y)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
CHOLECALCIFEROL (UNII: 1C6V77QF41)
SODIUM PROPOXYHYDROXYPROPYL THIOSULFATE SILICA (UNII: 208G222332)
EDETATE DISODIUM (UNII: 7FLD91C86K)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77375-005-01	50 g in 1 CONTAINER; Type 0: Not a Combination Product	06/04/2020	12/09/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	06/04/2020	12/09/2025

Labeler - Evora Worldwide (081336028)

Establishment
Name	Address	ID/FEI	Business Operations
Inspec Solution		081030372	manufacture(77375-005)

Revised: 12/2025

Document Id: 45c72375-1d7b-aa3c-e063-6294a90a620a

34390-5

Set id: 453196f3-4858-4b5c-bbd3-3e757b36b4fb

Version: 4

Effective Time: 20251212