NDC 70919-001 Ultra Shade Sunscreen Spf 30 Taheri Md
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70919 - La Laser Cente, Pc, California Professional Medical Corp
- 70919-001 - Ultra Shade Sunscreen Spf 30
Product Packages
NDC Code 70919-001-01
Package Description: 50 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 70919-001?
What are the uses for Ultra Shade Sunscreen Spf 30 Taheri Md?
Which are Ultra Shade Sunscreen Spf 30 Taheri Md UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Ultra Shade Sunscreen Spf 30 Taheri Md 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:
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- WATER (UNII: 059QF0KO0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- COCONUT ALKANES (UNII: 1E5KJY107T)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- LAURETH-7 (UNII: Z95S6G8201)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TROLAMINE (UNII: 9O3K93S3TK)
- XANTHAN GUM (UNII: TTV12P4NEE)
* 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".