NDC 42507-262 Le Techniq Hand Sanitizer Apple Pomegranate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42507 - Hyvee Inc
- 42507-262 - Le Techniq
Product Packages
NDC Code 42507-262-02
Package Description: 59 mL in 1 BOTTLE, PLASTIC
NDC Code 42507-262-09
Package Description: 259 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 42507-262?
What are the uses for Le Techniq Hand Sanitizer Apple Pomegranate?
Which are Le Techniq Hand Sanitizer Apple Pomegranate 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 Hand Sanitizer Apple Pomegranate 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)
- SULISOBENZONE (UNII: 1W6L629B4K)
- MANNITOL (UNII: 3OWL53L36A)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
What is the NDC to RxNorm Crosswalk for Le Techniq Hand Sanitizer Apple Pomegranate?
- 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".