NDC 52891-105 Dr. Oberon Original Snail Cream
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 52891-105?
Which are Dr. Oberon Original Snail Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Dr. Oberon Original Snail Cream 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:
- SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A)
- WATER (UNII: 059QF0KO0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ETHOHEXADIOL (UNII: M9JGK7U88V)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- GLYCERIN (UNII: PDC6A3C0OX)
- NIACINAMIDE (UNII: 25X51I8RD4)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)
- TRIDECETH-6 (UNII: 3T5PCR2H0C)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- CORNUS OFFICINALIS FRUIT (UNII: 23NL8NQ187)
- PRUNUS MUME FRUIT (UNII: 639190I8CU)
- PUNICA GRANATUM WHOLE (UNII: O2ZTS50U5E)
- ALLANTOIN (UNII: 344S277G0Z)
- ADENOSINE (UNII: K72T3FS567)
- PANTHENOL (UNII: WV9CM0O67Z)
- BENZOPHENONE-5 (UNII: 853Z42ZYAS)
- DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
- LAVANDULA ANGUSTIFOLIA WHOLE (UNII: 51217XIL5L)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CARAMEL (UNII: T9D99G2B1R)
* Please review the disclaimer below.
[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".