NDC 65364-401 Kiss My Face Sensitive
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 65364-401?
What are the uses for Kiss My Face Sensitive?
Which are Kiss My Face Sensitive UNII Codes?
The UNII codes for the active ingredients in this product are:
- POTASSIUM NITRATE (UNII: RU45X2JN0Z)
- NITRATE ION (UNII: T93E9Y2844) (Active Moiety)
Which are Kiss My Face 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:
- WATER (UNII: 059QF0KO0R)
- CETRARIA ISLANDICA SUBSP. ISLANDICA (UNII: BJ7YPN79A1)
- SODIUM LAURYL SARCOSINATE (UNII: 5PGH842FAU)
- SORBITOL (UNII: 506T60A25R)
- AESCULUS HIPPOCASTANUM SEED OIL (UNII: E0M52HIR1Y)
- TEA TREE OIL (UNII: VIF565UC2G)
- GLYCERIN (UNII: PDC6A3C0OX)
- XANTHAN GUM (UNII: TTV12P4NEE)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- OLEA EUROPAEA LEAF (UNII: MJ95C3OH47)
- SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ECHINACEA ANGUSTIFOLIA LEAF (UNII: FS7G8S6PJ8)
- MENTHOL (UNII: L7T10EIP3A)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- XYLITOL (UNII: VCQ006KQ1E)
- SODIUM COPPER CHLOROPHYLLIN (UNII: 1D276TYV9O)
- STEVIA REBAUDIUNA LEAF (UNII: 6TC6NN0876)
- MENTHA PIPERITA (UNII: 79M2M2UDA9)
- GLYCYRRHIZIN (UNII: 6FO62043WK)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
What is the NDC to RxNorm Crosswalk for Kiss My Face Sensitive?
- RxCUI: 312544 - potassium nitrate 5 % Toothpaste
- RxCUI: 312544 - potassium nitrate 0.05 MG/MG Toothpaste
- RxCUI: 312544 - K+ nitrate 0.05 MG/MG Toothpaste
- RxCUI: 312544 - Pot nitrate 0.05 MG/MG Toothpaste
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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".