NDC 70602-006 Exoden Sensitive
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70602 - Lifeon Corp.
- 70602-006 - Exoden Sensitive
Product Packages
NDC Code 70602-006-02
Package Description: 1 TUBE in 1 CARTON / 120 g in 1 TUBE (70602-006-01)
Product Details
What is NDC 70602-006?
What are the uses for Exoden Sensitive?
Which are Exoden Sensitive UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICALCIUM PHOSPHATE (UNII: K4C08XP666)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
Which are Exoden Sensitive 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)
- SORBITOL SOLUTION (UNII: 8KW3E207O2)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- XYLITOL (UNII: VCQ006KQ1E)
- GLUCOSYL STEVIOL (UNII: TKD5UC898Q)
- LICORICE (UNII: 61ZBX54883)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHAMOMILE (UNII: FGL3685T2X)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- CLARY SAGE (UNII: U3HSK5JC0Q)
- GENTIANA LUTEA ROOT (UNII: S72O3284MS)
- SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- LEVOMENTHOL (UNII: BZ1R15MTK7)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- ANETHOLE (UNII: Q3JEK5DO4K)
- CARVONE, (+/-)- (UNII: 75GK9XIA8I)
- CHAMAECYPARIS OBTUSA WOOD OIL (UNII: P2OMP71Y62)
- POTASSIUM NITRATE (UNII: RU45X2JN0Z)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Exoden Sensitive?
- RxCUI: 1374795 - tricalcium phosphate 19 % / silicon dioxide 2.5 % Toothpaste
- RxCUI: 1374795 - silicon dioxide 0.025 MG/MG / tricalcium phosphate 0.19 MG/MG Toothpaste
- RxCUI: 1374795 - silicon dioxide 2.5 % / tricalcium phosphate 19 % Toothpaste
* 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".