Label: CHIGGER RELIEF EVORA LABS- benzocaine 10% ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 77375-005-01 - Packager: Evora Worldwide
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated January 14, 2022
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- Official Label (Printer Friendly)
- Active ingredient Purpose
- PURPOSE
- Uses
- WarningsFor external use only.
- Keep out of reach of children
- Directions
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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?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CHIGGER RELIEF EVORA LABS
benzocaine 10% ointmentProduct 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 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 06/04/2020 Labeler - Evora Worldwide (081336028) Establishment Name Address ID/FEI Business Operations Inspec Solution 081030372 manufacture(77375-005)