NDC 75757-112 Cyber Clean Moisturizing Hand Sanitizer Eucalyptus
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75757 - Joker Ag
- 75757-112 - Cyber Clean Moisturizing Hand Sanitizer Eucalyptus
Product Packages
NDC Code 75757-112-01
Package Description: 175 mL in 1 BOTTLE
NDC Code 75757-112-02
Package Description: 450 mL in 1 BOTTLE
Product Details
What is NDC 75757-112?
What are the uses for Cyber Clean Moisturizing Hand Sanitizer Eucalyptus?
Which are Cyber Clean Moisturizing Hand Sanitizer Eucalyptus UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Cyber Clean Moisturizing Hand Sanitizer Eucalyptus 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:
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- TRIISOPROPANOLAMINE (UNII: W9EN9DLM98)
- CHROMIUM HYDROXIDE GREEN (UNII: RV8FT8XF5R)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CARBOMER 980 (UNII: 4Q93RCW27E)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- JOJOBA OIL (UNII: 724GKU717M)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Cyber Clean Moisturizing Hand Sanitizer Eucalyptus?
- RxCUI: 1052530 - ethanol 72 % Topical Solution
- RxCUI: 1052530 - ethanol 0.72 ML/ML 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".