NDC 24488-036 Bio 2 Brazilian Heat Brazilian Heat
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 24488 - Bio 2
- 24488-036 - Bio 2 Brazilian Heat
Product Packages
NDC Code 24488-036-74
Package Description: 60 mL in 1 BOTTLE, WITH APPLICATOR
Product Details
What is NDC 24488-036?
What are the uses for Bio 2 Brazilian Heat Brazilian Heat?
Which are Bio 2 Brazilian Heat Brazilian Heat UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Bio 2 Brazilian Heat Brazilian Heat 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:
- ALCOHOL (UNII: 3K9958V90M)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- GELIDIELLA ACEROSA (UNII: T91K54D6M1)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- CHLORINE DIOXIDE (UNII: 8061YMS4RM)
- HYPNEA MUSCIFORMIS (UNII: W6FF9R1FJV)
- MAGNESIUM (UNII: I38ZP9992A)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- SARGASSUM FILIPENDULA (UNII: 55P66J5H7N)
- SODIUM (UNII: 9NEZ333N27)
- SORBITOL (UNII: 506T60A25R)
- WATER (UNII: 059QF0KO0R)
- ZINC (UNII: J41CSQ7QDS)
What is the NDC to RxNorm Crosswalk for Bio 2 Brazilian Heat Brazilian Heat?
- RxCUI: 1086713 - menthol 7 % Topical Spray
- RxCUI: 1086713 - menthol 70 MG/ML Topical Spray
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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".