NDC 42681-0036 365 Whole Foods Market Anticavity/antigingivitis Mouthwash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42681 - Whole Foods Market, Inc.
- 42681-0036 - 365 Whole Foods Market Anticavity/antigingivitis Mouthwash
Product Characteristics
Product Packages
NDC Code 42681-0036-1
Package Description: 946 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 42681-0036?
What are the uses for 365 Whole Foods Market Anticavity/antigingivitis Mouthwash?
Which are 365 Whole Foods Market Anticavity/antigingivitis Mouthwash UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- THYMOL (UNII: 3J50XA376E)
- THYMOL (UNII: 3J50XA376E) (Active Moiety)
- EUCALYPTOL (UNII: RV6J6604TK)
- EUCALYPTOL (UNII: RV6J6604TK) (Active Moiety)
Which are 365 Whole Foods Market Anticavity/antigingivitis Mouthwash 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:
- SORBITOL (UNII: 506T60A25R)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- SPEARMINT OIL (UNII: C3M81465G5)
- STEVIA LEAF (UNII: 6TC6NN0876)
* Please review the disclaimer below.
[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".