NDC 79489-0010 Cc Cream Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 79489-0010?
What are the uses for Cc Cream Spf 30?
Which are Cc Cream Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Cc Cream Spf 30 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:
- COCONUT ALKANES (UNII: 1E5KJY107T)
- COCONUT OIL (UNII: Q9L0O73W7L)
- TRICAPRILIN (UNII: 6P92858988)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CASTOR OIL (UNII: D5340Y2I9G)
- ETHYL MACADAMIATE (UNII: ANA2NCS6V1)
- GLYCERIN (UNII: PDC6A3C0OX)
- ORANGE PEEL WAX (UNII: 0U715N387C)
- JOJOBA OIL (UNII: 724GKU717M)
- COCOYL CAPRYLOCAPRATE (UNII: 8D9H4QU99H)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- SHEA BUTTER (UNII: K49155WL9Y)
- TOCOPHEROL (UNII: R0ZB2556P8)
- CAPRIC ACID (UNII: 4G9EDB6V73)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- KAOLIN (UNII: 24H4NWX5CO)
- ARGAN OIL (UNII: 4V59G5UW9X)
- ROSA MOSCHATA OIL (UNII: J99W255AWF)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- OREGANO (UNII: 0E5AT8T16U)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- LEVOMENOL (UNII: 24WE03BX2T)
- MALIC ACID (UNII: 817L1N4CKP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
* 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".