NDC 59735-130 Daily Moisturizer Broad-spectrum Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59735 - Mana Products
- 59735-130 - Daily Moisturizer Broad-spectrum Spf 30
Product Packages
NDC Code 59735-130-01
Package Description: 50 g in 1 TUBE
Product Details
What is NDC 59735-130?
What are the uses for Daily Moisturizer Broad-spectrum Spf 30?
Which are Daily Moisturizer Broad-spectrum Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Daily Moisturizer Broad-spectrum 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:
- WATER (UNII: 059QF0KO0R)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- MICA (UNII: V8A1AW0880)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- GLYCERIN (UNII: PDC6A3C0OX)
- SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H)
- SHEA BUTTER (UNII: K49155WL9Y)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- BEHENYL BENZOATE (UNII: DQG8119XKJ)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- MYRISTYL ALCOHOL (UNII: V42034O9PU)
- LAURYL ALCOHOL (UNII: 178A96NLP2)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- PALMITIC ACID (UNII: 2V16EO95H1)
- COCO GLUCOSIDE (UNII: ICS790225B)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- PRUNUS ARMENIACA LEAF (UNII: 0X5YG5R83N)
- CARICA PAPAYA LEAF (UNII: 66J7636Z2I)
- CYMBOPOGON SCHOENANTHUS OIL (UNII: XE7K568ILO)
- AESCULUS HIPPOCASTANUM LEAF (UNII: Z49U891FNQ)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- PROPYLENE GLYCOL STEARATE (UNII: MZM1I680W0)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- SODIUM HYDRIDE (UNII: 23J3BHR95O)
- PROPYLENE GLYCOL LAURATES (UNII: 40KT317HGP)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- O-CYMEN-5-OL (UNII: H41B6Q1I9L)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BENZYL SALICYLATE (UNII: WAO5MNK9TU)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- LIMONENE, DL- (UNII: 9MC3I34447)
* 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".