NDC 70990-003 Ethereal Skin Calming Moisturizing Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70990 - Donegal Bay Ltd
- 70990-003 - Ethereal Skin Calming Moisturizing Cream
Product Packages
NDC Code 70990-003-01
Package Description: 252 mL in 1 TUBE
Product Details
What is NDC 70990-003?
What are the uses for Ethereal Skin Calming Moisturizing Cream?
Which are Ethereal Skin Calming Moisturizing Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Ethereal Skin Calming Moisturizing 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:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- MINERAL OIL (UNII: T5L8T28FGP)
- CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- PEG-40 STEARATE (UNII: ECU18C66Q7)
- CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
What is the NDC to RxNorm Crosswalk for Ethereal Skin Calming Moisturizing Cream?
- RxCUI: 244642 - dimethicone 2 % Topical Cream
- RxCUI: 244642 - dimethicone 20 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".