NDC 50950-001 Iman Time Control All Day Moisture Complex Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50950 - Sheencolor Biotech Co., Ltd.
- 50950-001 - Iman Time Control All Day Moisture Complex Spf 15
Product Packages
NDC Code 50950-001-01
Package Description: 89 g in 1 TUBE
Product Details
What is NDC 50950-001?
What are the uses for Iman Time Control All Day Moisture Complex Spf 15?
Which are Iman Time Control All Day Moisture Complex Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Iman Time Control All Day Moisture Complex Spf 15 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- POLYOXYL 100 STEARATE (UNII: YD01N1999R)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- APRICOT SEED OIL (UNII: 54JB35T06A)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- GINKGO (UNII: 19FUJ2C58T)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- TROLAMINE (UNII: 9O3K93S3TK)
- CARBOMER HOMOPOLYMER TYPE A (UNII: F68VH75CJC)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ETHYLPARABEN (UNII: 14255EXE39)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ENGLISH LAVENDER OIL (UNII: ZBP1YXW0H8)
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[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".