NDC 50184-6400 Hope In A Jar For Dry Skin Spf Broad Spectrum Spf 20 Sunscreen And Extra-rich Moisturizer For Normal To Dry Skin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50184 - Philosophy, Inc.
- 50184-6400 - Hope In A Jar For Dry Skin Spf
Product Packages
NDC Code 50184-6400-2
Package Description: 1 TUBE in 1 BOX / 60 mL in 1 TUBE (50184-6400-1)
Product Details
What is NDC 50184-6400?
What are the uses for Hope In A Jar For Dry Skin Spf Broad Spectrum Spf 20 Sunscreen And Extra-rich Moisturizer For Normal To Dry Skin?
Which are Hope In A Jar For Dry Skin Spf Broad Spectrum Spf 20 Sunscreen And Extra-rich Moisturizer For Normal To Dry Skin 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)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Hope In A Jar For Dry Skin Spf Broad Spectrum Spf 20 Sunscreen And Extra-rich Moisturizer For Normal To Dry Skin 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)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- DOCOSANOIC ACID (UNII: H390488X0A)
- GLYCERIN (UNII: PDC6A3C0OX)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- DOCOSANOL (UNII: 9G1OE216XY)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ENGLISH LAVENDER OIL (UNII: ZBP1YXW0H8)
- 1,3-BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CARBOMER 934 (UNII: Z135WT9208)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- ARGININE (UNII: 94ZLA3W45F)
- SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
- TROLAMINE (UNII: 9O3K93S3TK)
- CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- SQUALENE (UNII: 7QWM220FJH)
- RICE BRAN (UNII: R60QEP13IC)
- METHYLDIBROMO GLUTARONITRILE (UNII: YX089CPS05)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
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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".