NDC 90107-2420 The Itch Eraser Sensitive
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 90107 - Adventure Ready Brands
- 90107-2420 - The Itch Eraser Sensitive
Product Packages
NDC Code 90107-2420-1
Package Description: 4 TUBE in 1 BOX / 20 g in 1 TUBE
Product Details
What is NDC 90107-2420?
What are the uses for The Itch Eraser Sensitive?
Which are The Itch Eraser Sensitive UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
Which are The Itch Eraser 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL)
- OLETH-10 (UNII: JD797EF70J)
- PHOSPHATE ION (UNII: NK08V8K8HR)
- WATER (UNII: 059QF0KO0R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TEA TREE OIL (UNII: VIF565UC2G)
What is the NDC to RxNorm Crosswalk for The Itch Eraser Sensitive?
- RxCUI: 1722238 - sodium bicarbonate 5 % Topical Cream
- RxCUI: 1722238 - sodium bicarbonate 50 MG/ML Topical Cream
- RxCUI: 1722238 - NaHCO3 50 MG/ML Topical Cream
- RxCUI: 1724479 - The Itch Eraser Sensitive 5 % Topical Cream
- RxCUI: 1724479 - sodium bicarbonate 50 MG/ML Topical Cream [The Itch Eraser Sensitive]
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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".