NDC 61924-410 Renew Dimethicone Skin Protectant
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61924 - Dermarite Industries Llc
- 61924-410 - Renew Dimethicone Skin Protectant
Product Characteristics
Product Packages
NDC Code 61924-410-04
Package Description: 113 g in 1 TUBE
NDC Code 61924-410-05
Package Description: 5 g in 1 PACKET
Product Details
What is NDC 61924-410?
What are the uses for Renew Dimethicone Skin Protectant?
Which are Renew Dimethicone Skin Protectant UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Renew Dimethicone Skin Protectant 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- CANOLA OIL (UNII: 331KBJ17RK)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- ETHYLPARABEN (UNII: 14255EXE39)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- NIACINAMIDE (UNII: 25X51I8RD4)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TROLAMINE (UNII: 9O3K93S3TK)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- WATER (UNII: 059QF0KO0R)
- CORN OIL (UNII: 8470G57WFM)
* 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".