NDC 82951-001 The Davinci Company
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 82951-001?
What are the uses for The Davinci Company?
Which are The Davinci Company UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are The Davinci Company 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)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- LYSINE HYDROCHLORIDE (UNII: JNJ23Q2COM)
- TRICAPRYLIN (UNII: 6P92858988)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)
- PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM PROPOXYHYDROXYPROPYL THIOSULFATE SILICA (UNII: 208G222332)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- MINERAL OIL (UNII: T5L8T28FGP)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HYDROCORTISONE (UNII: WI4X0X7BPJ)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PEG-8 DIMETHICONE (UNII: GIA7T764OD)
- PETROLATUM (UNII: 4T6H12BN9U)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
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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".