NDC 73690-027 Versed Guards Up Daily Mineral Sunscreen Broad Spectrum Spf 35
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What is NDC 73690-027?
What are the uses for Versed Guards Up Daily Mineral Sunscreen Broad Spectrum Spf 35?
Which are Versed Guards Up Daily Mineral Sunscreen Broad Spectrum Spf 35 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Versed Guards Up Daily Mineral Sunscreen Broad Spectrum Spf 35 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:
- C18-C21 ALKANE (UNII: 33822S0M40)
- ERYTHRITOL (UNII: RA96B954X6)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- COCO GLUCOSIDE (UNII: ICS790225B)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- DOCOSANOL (UNII: 9G1OE216XY)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- PROPANEDIOL (UNII: 5965N8W85T)
- GLYCERIN (UNII: PDC6A3C0OX)
- APPLE (UNII: B423VGH5S9)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CRITHMUM MARITIMUM WHOLE (UNII: J7IHY79BKY)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- ISODECYL NEOPENTANOATE (UNII: W60VYE24XC)
- DIHEPTYL SUCCINATE (UNII: 057N7SS26Y)
- CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- LEVOMENOL (UNII: 24WE03BX2T)
- HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
- SODIUM GLUCONATE (UNII: R6Q3791S76)
- OCTYLDODECYL OLEATE (UNII: MCA43PK7MH)
- WATER (UNII: 059QF0KO0R)
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- TOCOPHEROL (UNII: R0ZB2556P8)
- ETHYL FERULATE (UNII: 5B8915UELW)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
* 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".