NDC 75814-103 Allout Nano
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Product Details
What is NDC 75814-103?
What are the uses for Allout Nano?
Which are Allout Nano UNII Codes?
The UNII codes for the active ingredients in this product are:
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)
Which are Allout Nano 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:
- POTASSIUM ALUM (UNII: 1L24V9R23S)
- SILVER (UNII: 3M4G523W1G)
- COPPER (UNII: 789U1901C5)
- PYRITHIONE ZINC (UNII: R953O2RHZ5)
- CAMPHOR OIL, WHITE (UNII: 26P3H26Z9X)
- HYALURONIC ACID (UNII: S270N0TRQY)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERIN (UNII: PDC6A3C0OX)
What is the NDC to RxNorm Crosswalk for Allout Nano?
- RxCUI: 1598066 - isopropyl alcohol 75 % Topical Spray
- RxCUI: 1598066 - isopropyl alcohol 0.75 ML/ML Topical Spray
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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".