NDC 42248-132 Firming And Moisturizing Body
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 42248-132?
Which are Firming And Moisturizing Body UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Firming And Moisturizing Body 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- PEG-8 STEARATE (UNII: 2P9L47VI5E)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- PEG-6 STEARATE (UNII: 8LQC57C6B0)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- LAMINARIA DIGITATA (UNII: 15E7C67EE8)
- HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)
- CETEARYL ISONONANOATE (UNII: P5O01U99NI)
- SOYBEAN (UNII: L7HT8F1ZOD)
- CHONDRUS CRISPUS (UNII: OQS23HUA1X)
- CARBOMER HOMOPOLYMER TYPE B/C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- ALLANTOIN (UNII: 344S277G0Z)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ETHYLPARABEN (UNII: 14255EXE39)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- PEG-32 STEARATE (UNII: 33GX5WQC0M)
- EUROPEAN HAZELNUT OIL (UNII: 8RQ2839AVG)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- EDETIC ACID (UNII: 9G34HU7RV0)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CUCUMBER (UNII: YY7C30VXJT)
- UREA (UNII: 8W8T17847W)
- ARNICA MONTANA (UNII: O80TY208ZW)
- IMIDUREA (UNII: M629807ATL)
- BOMBYX MORI FIBER (UNII: 6LK42KUV6W)
- FISH SKIN COLLAGEN, SOLUBLE (UNII: 8JC99XGU4W)
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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".