NDC 65753-102 Sun X Multi-pack Spf 30 Thick
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65753 - Coretex Products Inc
- 65753-102 - Sun X Multi-pack Spf 30 Thick
Product Packages
NDC Code 65753-102-22
Package Description: 25 POUCH in 1 CONTAINER / 7 g in 1 POUCH
NDC Code 65753-102-23
Package Description: 25 POUCH in 1 CONTAINER / 7 g in 1 POUCH
NDC Code 65753-102-24
Package Description: 50 POUCH in 1 CONTAINER / 7 g in 1 POUCH
NDC Code 65753-102-26
Package Description: 300 POUCH in 1 BOX / 7 g in 1 POUCH
NDC Code 65753-102-31
Package Description: 150 POUCH in 1 BOX / 7 g in 1 POUCH
Product Details
What is NDC 65753-102?
What are the uses for Sun X Multi-pack Spf 30 Thick?
Which are Sun X Multi-pack Spf 30 Thick UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Sun X Multi-pack Spf 30 Thick 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:
- METHYLPARABEN (UNII: A2I8C7HI9T)
- C12-20 ALKYL BENZOATE (UNII: Y15I6XI14C)
- EDETIC ACID (UNII: 9G34HU7RV0)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ETHYLPARABEN (UNII: 14255EXE39)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- TROLAMINE (UNII: 9O3K93S3TK)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CARBOMER HOMOPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: F68VH75CJC)
- WATER (UNII: 059QF0KO0R)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- DIMETHYL CAPRAMIDE (UNII: O29Y6X2JEZ)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- NASTURTIUM OFFICINALE (UNII: YH89GMV676)
- COMFREY LEAF (UNII: DG4F8T839X)
- CHAMOMILE (UNII: FGL3685T2X)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
* 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".