NDC 28851-694 Kendall Moisturizing
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 28851 - Covidien Inc.
- 28851-694 - Kendall Moisturizing
Product Packages
NDC Code 28851-694-01
Package Description: 59 mL in 1 TUBE
NDC Code 28851-694-02
Package Description: 118 mL in 1 TUBE
NDC Code 28851-694-03
Package Description: 4 mL in 1 POUCH
Product Details
What is NDC 28851-694?
What are the uses for Kendall Moisturizing?
Which are Kendall Moisturizing UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Kendall Moisturizing 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)
- 1-DECENE (UNII: 7O4U4C718P)
- 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 Moisturizing?
- RxCUI: 200090 - dimethicone 1.5 % Topical Lotion
- RxCUI: 200090 - dimethicone 15 MG/ML Topical Lotion
* 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".