NDC 71712-001 Clean Fresh Sunblock Sunscreen Spf 30 Continuous
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71712 - Wuxi Huoban Daily-use Chemical Science And Technology Co., Ltd.
- 71712-001 - Clean Fresh Sunblock Sunscreen Spf 30 Continuous
Product Packages
NDC Code 71712-001-01
Package Description: 150 mL in 1 BOTTLE
Product Details
What is NDC 71712-001?
What are the uses for Clean Fresh Sunblock Sunscreen Spf 30 Continuous?
Which are Clean Fresh Sunblock Sunscreen Spf 30 Continuous 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)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Clean Fresh Sunblock Sunscreen Spf 30 Continuous 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)
- SORBITOL (UNII: 506T60A25R)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- TOCOPHEROL (UNII: R0ZB2556P8)
- POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- DISODIUM HEDTA (UNII: KME849MC7A)
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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".