NDC 78936-010 Bb1720d Antibacterial Hand Wipes Hawaiian Coconut Scented Bb1720d
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 78936 - Hangzhou Caring Cleaning Commodity Co.,ltd
- 78936-010 - Bb1720d Antibacterial Hand Wipes Hawaiian Coconut Scented
Product Packages
NDC Code 78936-010-01
Package Description: 50 POUCH in 1 PACKAGE / 1 g in 1 POUCH
NDC Code 78936-010-02
Package Description: 75 POUCH in 1 PAIL / 1 g in 1 POUCH
NDC Code 78936-010-03
Package Description: 20 POUCH in 1 BOX / 1 g in 1 POUCH
Product Details
What is NDC 78936-010?
What are the uses for Bb1720d Antibacterial Hand Wipes Hawaiian Coconut Scented Bb1720d?
Which are Bb1720d Antibacterial Hand Wipes Hawaiian Coconut Scented Bb1720d UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Bb1720d Antibacterial Hand Wipes Hawaiian Coconut Scented Bb1720d 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- WATER (UNII: 059QF0KO0R)
- FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)
What is the NDC to RxNorm Crosswalk for Bb1720d Antibacterial Hand Wipes Hawaiian Coconut Scented Bb1720d?
- RxCUI: 1307051 - ethanol 75 % Medicated Pad
- RxCUI: 1307051 - ethanol 0.75 ML/ML Medicated Pad
- RxCUI: 1307051 - ethanol 75 % Hand Sanitizer Wipes
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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".