NDC 83872-093 Brazilian Bum Bum Cream
Bum Bum Cream Cream Topical - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 83872-093?
What are the uses for Brazilian Bum Bum Cream?
What are Brazilian Bum Bum Cream Active Ingredients?
- ASCORBIC ACID 20 mg/g - A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant.
- BERTHOLLETIA EXCELSA FLOWER 10 mg/g
- CAMELLIA SINENSIS FLOWER 10 mg/g
- CARROT SEED OIL 10 mg/g
- CERAMIDE NP 10 mg/g
- EUTERPE OLERACEA WHOLE 10 mg/g
- HYALURONIC ACID 10 mg/g - A natural high-viscosity mucopolysaccharide with alternating beta (1-3) glucuronide and beta (1-4) glucosaminidic bonds. It is found in the UMBILICAL CORD, in VITREOUS BODY and in SYNOVIAL FLUID. A high urinary level is found in PROGERIA.
- LAVANDULA ANGUSTIFOLIA FLOWER 10 mg/g
- MATRICARIA RECUTITA FLOWERING TOP 10 mg/g
- PALMITOYL TETRAPEPTIDE-7 10 mg/g
- PUNICA GRANATUM FLOWER 10 mg/g
- RETINOL 10 mg/g
- ROSMARINUS OFFICINALIS FLOWER 10 mg/g
- THEOBROMA GRANDIFLORUM SEED BUTTER 10 mg/g
- TOCOPHEROL 15 mg/g
Which are Brazilian Bum Bum Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M) (Active Moiety)
- ROSMARINUS OFFICINALIS FLOWER (UNII: NR1A27F29O)
- ROSMARINUS OFFICINALIS FLOWER (UNII: NR1A27F29O) (Active Moiety)
- PUNICA GRANATUM FLOWER (UNII: D9B634V4GP)
- PUNICA GRANATUM FLOWER (UNII: D9B634V4GP) (Active Moiety)
- THEOBROMA GRANDIFLORUM SEED BUTTER (UNII: I711F13FXM)
- THEOBROMA GRANDIFLORUM SEED BUTTER (UNII: I711F13FXM) (Active Moiety)
- BERTHOLLETIA EXCELSA FLOWER (UNII: NI60Y19CKF)
- BERTHOLLETIA EXCELSA FLOWER (UNII: NI60Y19CKF) (Active Moiety)
- CARROT SEED OIL (UNII: 595AO13F11)
- CARROT SEED OIL (UNII: 595AO13F11) (Active Moiety)
- RETINOL (UNII: G2SH0XKK91)
- RETINOL (UNII: G2SH0XKK91) (Active Moiety)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TOCOPHEROL (UNII: R0ZB2556P8) (Active Moiety)
- MATRICARIA RECUTITA FLOWERING TOP (UNII: 3VNC7T6Z02)
- MATRICARIA RECUTITA FLOWERING TOP (UNII: 3VNC7T6Z02) (Active Moiety)
- CERAMIDE NP (UNII: 4370DF050B)
- CERAMIDE NP (UNII: 4370DF050B) (Active Moiety)
- CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17)
- CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17) (Active Moiety)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R) (Active Moiety)
- HYALURONIC ACID (UNII: S270N0TRQY)
- HYALURONIC ACID (UNII: S270N0TRQY) (Active Moiety)
- EUTERPE OLERACEA WHOLE (UNII: Y57H6218HP)
- EUTERPE OLERACEA WHOLE (UNII: Y57H6218HP) (Active Moiety)
Which are Brazilian Bum Bum Cream 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:
- ORYZA SATIVA WHOLE (UNII: 84IVV0906Z)
- WATER (UNII: 059QF0KO0R)
- PANTHENOL (UNII: WV9CM0O67Z)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- XANTHAN GUM (UNII: TTV12P4NEE)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- COCONUT OIL (UNII: Q9L0O73W7L)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- SYNTHETIC BEESWAX (UNII: 08MNR5YE2R)
Which are the Pharmacologic Classes for Brazilian Bum Bum Cream?
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[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 ("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".