NDC 51706-956 Weclean Hand Sanitizer Lemon Scent
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51706 - Landy International
- 51706-956 - Weclean Hand Sanitizer Lemon Scent
Product Packages
NDC Code 51706-956-01
Package Description: 250 mL in 1 BOTTLE
Product Details
What is NDC 51706-956?
What are the uses for Weclean Hand Sanitizer Lemon Scent?
Which are Weclean Hand Sanitizer Lemon Scent UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Weclean Hand Sanitizer Lemon Scent 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:
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- TROLAMINE (UNII: 9O3K93S3TK)
- JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL)
- LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Weclean Hand Sanitizer Lemon Scent?
- RxCUI: 581660 - ethanol 62 % Topical Gel
- RxCUI: 581660 - ethanol 0.62 ML/ML Topical Gel
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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".