NDC 50638-100 Maxxima
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50638 - Dr. Knoll Products, Inc.
- 50638-100 - Maxxima
Product Packages
NDC Code 50638-100-02
Package Description: 60 mL in 1 BOTTLE
NDC Code 50638-100-04
Package Description: 120 mL in 1 BOTTLE
Product Details
What is NDC 50638-100?
What are the uses for Maxxima?
Which are Maxxima UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Maxxima 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- TEA TREE OIL (UNII: VIF565UC2G)
- PICEA MARIANA LEAF OIL (UNII: Q1J49L1A5O)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- SAGE OIL (UNII: U27K0H1H2O)
- JUNIPER BERRY OIL (UNII: SZH16H44UY)
- CAJUPUT OIL (UNII: J3TO6BUQ37)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- SODIUM COPPER CHLOROPHYLLIN (UNII: 1D276TYV9O)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
What is the NDC to RxNorm Crosswalk for Maxxima?
- RxCUI: 1999327 - camphor 3.01 % / menthol 1.25 % Topical Cream
- RxCUI: 1999327 - camphor 30.1 MG/ML / menthol 12.5 MG/ML Topical Cream
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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".