NDC 52554-1112 Powerproof Sunscreen 100
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52554 - Cms Lab Inc.
- 52554-1112 - Powerproof Sunscreen 100
Product Packages
NDC Code 52554-1112-2
Package Description: 1 TUBE in 1 PACKAGE / 50 mL in 1 TUBE (52554-1112-1)
Product Details
What is NDC 52554-1112?
What are the uses for Powerproof Sunscreen 100?
Which are Powerproof Sunscreen 100 UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Powerproof Sunscreen 100 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)
- HEXAMETHYLDISILOXANE (UNII: D7M4659BPU)
- ALCOHOL (UNII: 3K9958V90M)
- METHICONE (20 CST) (UNII: 6777U11MKT)
- DIBUTYL ADIPATE (UNII: F4K100DXP3)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- POLYSILICONE-15 (UNII: F8DRP5BB29)
- DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
- PROPANEDIOL (UNII: 5965N8W85T)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- PURSLANE (UNII: M6S840WXG5)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- CALCIUM ALUMINUM BOROSILICATE (UNII: 3JRB8A35M0)
- INVERT SUGAR (UNII: ED959S6ACY)
- TURMERIC (UNII: 856YO1Z64F)
- CHIA SEED (UNII: NU0OLX06F8)
* 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".