NDC 42507-058 Le Techniq Antibacterial Hand Island Citrus
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42507 - Hyvee Inc
- 42507-058 - Le Techniq
Product Packages
NDC Code 42507-058-02
Package Description: 59 mL in 1 BOTTLE, PLASTIC
NDC Code 42507-058-09
Package Description: 259 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 42507-058?
What are the uses for Le Techniq Antibacterial Hand Island Citrus?
Which are Le Techniq Antibacterial Hand Island Citrus UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Le Techniq Antibacterial Hand Island Citrus 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)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CARBOMER 934 (UNII: Z135WT9208)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- MANNITOL (UNII: 3OWL53L36A)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- CHROMIUM HYDROXIDE GREEN (UNII: RV8FT8XF5R)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Le Techniq Antibacterial Hand Island Citrus?
- RxCUI: 247835 - ethanol 62 % Topical Solution
- RxCUI: 247835 - ethanol 0.62 ML/ML Topical Solution
- RxCUI: 247835 - ethyl alcohol 62 % Topical Solution
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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".