NDC 77375-005 Chigger Relief Evora Labs
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 77375-005?
What are the uses for Chigger Relief Evora Labs?
Which are Chigger Relief Evora Labs UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
Which are Chigger Relief Evora Labs Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- 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)
What is the NDC to RxNorm Crosswalk for Chigger Relief Evora Labs?
- RxCUI: 197395 - benzocaine 10 % Topical Ointment
- RxCUI: 197395 - benzocaine 0.1 MG/MG Topical Ointment
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".