NDC 59240-003 Cold And Hot
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 59240-003?
What are the uses for Cold And Hot?
Which are Cold And Hot UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Cold And Hot 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)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CAPSAICIN (UNII: S07O44R1ZM)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CETYL ESTERS WAX (UNII: D072FFP9GU)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- CITRUS PARADISI FRUIT OIL (UNII: 6A7N43E0OJ)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- GLYCERIN (UNII: PDC6A3C0OX)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
- SPEARMINT (UNII: J7I2T6IV1N)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- PROPANEDIOL (UNII: 5965N8W85T)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- PEG-80 SORBITAN PALMITATE (UNII: 4NR71FN0IA)
- STEARETH-2 (UNII: V56DFE46J5)
- STEARETH-21 (UNII: 53J3F32P58)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Cold And Hot?
- RxCUI: 1091886 - menthol 7.5 % Topical Cream
- RxCUI: 1091886 - menthol 75 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".