NDC 24474-002 Run Guard Sensitive
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 24474 - Runguards Llc
- 24474-002 - Run Guard Sensitive
Product Packages
NDC Code 24474-002-01
Package Description: 76 g in 1 TUBE
NDC Code 24474-002-02
Package Description: 14 g in 1 TUBE
Product Details
What is NDC 24474-002?
What are the uses for Run Guard Sensitive?
Which are Run Guard Sensitive UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
Which are Run Guard 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)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- JOJOBA OIL (UNII: 724GKU717M)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- SHEA BUTTER (UNII: K49155WL9Y)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
What is the NDC to RxNorm Crosswalk for Run Guard Sensitive?
- RxCUI: 1044541 - allantoin 0.5 % Topical Ointment
- RxCUI: 1044541 - allantoin 0.005 MG/MG Topical Ointment
- RxCUI: 1044541 - allantoin 0.5 % Topical Stick
- RxCUI: 1547244 - Run Guard 0.5 % Topical Stick
- RxCUI: 1547244 - allantoin 0.005 MG/MG Topical Ointment [Run Guard]
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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".