NDC 28851-693 Kendall Moisture Barrier
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 28851-693?
What are the uses for Kendall Moisture Barrier?
Which are Kendall Moisture Barrier UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Kendall Moisture Barrier 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)
- JOJOBA OIL (UNII: 724GKU717M)
- STARCH, CORN (UNII: O8232NY3SJ)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BERGAMOT OIL (UNII: 39W1PKE3JI)
- TROLAMINE (UNII: 9O3K93S3TK)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- CARBOMER 1342 (UNII: 809Y72KV36)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- ETHYLPARABEN (UNII: 14255EXE39)
- SHEA BUTTER (UNII: K49155WL9Y)
- ACETATE ION (UNII: 569DQM74SC)
What is the NDC to RxNorm Crosswalk for Kendall Moisture Barrier?
- RxCUI: 259090 - dimethicone 5 % Topical Cream
- RxCUI: 259090 - dimethicone 50 MG/ML Topical Cream
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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".