NDC 11099-0004 Aloe Vesta Daily Moisturizer 118ml
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11099 - Guest Packaging Llc.
- 11099-0004 - Aloe Vesta Daily Moisturizer 118ml
Product Packages
NDC Code 11099-0004-4
Package Description: 118 mL in 1 BOTTLE
Product Details
What is NDC 11099-0004?
What are the uses for Aloe Vesta Daily Moisturizer 118ml?
Which are Aloe Vesta Daily Moisturizer 118ml UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Aloe Vesta Daily Moisturizer 118ml 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)
- PETROLATUM (UNII: 4T6H12BN9U)
- GLYCERIN (UNII: PDC6A3C0OX)
- STEARETH-2 (UNII: V56DFE46J5)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- LAURETH-23 (UNII: N72LMW566G)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
What is the NDC to RxNorm Crosswalk for Aloe Vesta Daily Moisturizer 118ml?
- RxCUI: 1485220 - ALOE VESTA Daily Moisturizer 3 % Topical Lotion
- RxCUI: 1485220 - dimethicone 30 MG/ML Topical Lotion [Aloe Vesta Daily Moisturizer]
- RxCUI: 1485220 - Aloe Vesta Daily Moisturizer 3 % Topical Lotion
- RxCUI: 1485220 - Aloe Vesta Daily Moisturizer 30 MG/ML Topical Lotion
- RxCUI: 309918 - dimethicone 3 % 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".