NDC 34834-003 Merino Collagen Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 34834 - Merino Lanolin Skin Care Products
- 34834-003 - Merino Collagen Spf 30
Product Packages
NDC Code 34834-003-01
Package Description: 100 g in 1 JAR
Product Details
What is NDC 34834-003?
What are the uses for Merino Collagen Spf 30?
Which are Merino Collagen Spf 30 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 Merino Collagen Spf 30 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)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- PEG-20 STEARATE (UNII: NBX892EA57)
- CYCLOMETHICONE 4 (UNII: CZ227117JE)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- MARINE COLLAGEN, SOLUBLE (UNII: 8JC99XGU4W)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- TROLAMINE (UNII: 9O3K93S3TK)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- LANOLIN (UNII: 7EV65EAW6H)
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
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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".