NDC 70738-001 Lagom Cellus Sun Gel
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 70738-001?
What are the uses for Lagom Cellus Sun Gel?
Which are Lagom Cellus Sun Gel UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Lagom Cellus Sun Gel 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)
- ALCOHOL (UNII: 3K9958V90M)
- PROPANEDIOL (UNII: 5965N8W85T)
- AVOBENZONE (UNII: G63QQF2NOX)
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- BIS-PEG/PPG-16/16 PEG/PPG-16/16 DIMETHICONE (UNII: 55A74AJ3KB)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ORANGE OIL (UNII: AKN3KSD11B)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GERANIUM MACULATUM ROOT OIL (UNII: H2E371EDYX)
- BERGAMOT OIL (UNII: 39W1PKE3JI)
- SANDALWOOD OIL (UNII: X7X01WMQ5F)
- ROSA RUGOSA FLOWER BUD (UNII: TZ0BE8I3MW)
- CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)
- UREA (UNII: 8W8T17847W)
- TREHALOSE (UNII: B8WCK70T7I)
- BETAINE (UNII: 3SCV180C9W)
- TAURINE (UNII: 1EQV5MLY3D)
- INOSITOL (UNII: 4L6452S749)
- STYRAX BENZOIN RESIN (UNII: FE663Z8IRO)
- MYRRH OIL (UNII: H74221J5J4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
* 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".