NDC 69678-101 Eez-away Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 69678-101?
What are the uses for Eez-away Relief?
Which are Eez-away Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Eez-away Relief 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)
- ALCOHOL (UNII: 3K9958V90M)
- IODINE (UNII: 9679TC07X4)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- POLYOXYL-10 OLEYL ETHER (UNII: JD797EF70J)
- PEG-75 LANOLIN (UNII: 09179OX7TB)
- PPG-20 METHYL GLUCOSE ETHER DISTEARATE (UNII: 0057334FAB)
- SODIUM IODIDE (UNII: F5WR8N145C)
- SODIUM THIOSULFATE (UNII: HX1032V43M)
What is the NDC to RxNorm Crosswalk for Eez-away Relief?
- RxCUI: 1606487 - menthol 1.25 % Topical Spray
- RxCUI: 1606487 - menthol 12.5 MG/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".