NDC 78362-801 Viiva Bioderma Actives
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Get all the details for National Drug Code (NDC) 78362-801 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.
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Product Details
What is NDC 78362-801?
What are the uses for Viiva Bioderma Actives?
Which are Viiva Bioderma Actives UNII Codes?
The UNII codes for the active ingredients in this product are:
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- THYROID, BOVINE (UNII: MN18OTN73W)
- THYROID, BOVINE (UNII: MN18OTN73W) (Active Moiety)
- SOMATROPIN (UNII: NQX9KB6PCL)
- SOMATROPIN (UNII: NQX9KB6PCL) (Active Moiety)
Which are Viiva Bioderma Actives 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)
- WATER (UNII: 059QF0KO0R)
- LICORICE (UNII: 61ZBX54883)
- CHASTE TREE FRUIT (UNII: 433OSF3U8A)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- GINKGO (UNII: 19FUJ2C58T)
- GAMMA ORYZANOL (UNII: SST9XCL51M)
- DIOSCOREA VILLOSA ROOT (UNII: IWY3IWX2G8)
- ACAI OIL (UNII: Z0W6766A2W)
- TAGETES MINUTA FLOWER OIL (UNII: 1T0ZMU8M8B)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- MUCUNA PRURIENS SEED (UNII: 55G8SQ543S)
- EPIMEDIUM SAGITTATUM TOP (UNII: 7G8Y7M4D58)
- COCONUT OIL (UNII: Q9L0O73W7L)
- JOJOBA OIL (UNII: 724GKU717M)
- PASSIFLORA EDULIS FLOWER (UNII: SY49TH8VUA)
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".