NDC 77442-003 (fruli) Hand Antiseptic Rinse Free Gel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 77442 - Shandong Zhuojian Medical Technology Co., Ltd.
- 77442-003 - (fruli) Hand Antiseptic Rinse Free Gel
Product Packages
NDC Code 77442-003-01
Package Description: 60 mL in 1 BOTTLE, DROPPER
NDC Code 77442-003-02
Package Description: 100 mL in 1 BOTTLE, DROPPER
NDC Code 77442-003-03
Package Description: 250 mL in 1 BOTTLE, DROPPER
NDC Code 77442-003-04
Package Description: 500 mL in 1 BOTTLE, DROPPER
NDC Code 77442-003-05
Package Description: 1000 mL in 1 BOTTLE, DROPPER
NDC Code 77442-003-06
Package Description: 5000 mL in 1 BOTTLE, DROPPER
NDC Code 77442-003-07
Package Description: 3 mL in 1 BAG
Product Details
What is NDC 77442-003?
What are the uses for (fruli) Hand Antiseptic Rinse Free Gel?
Which are (fruli) Hand Antiseptic Rinse Free Gel UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
- PROPYL ALCOHOL (UNII: 96F264O9SV)
- PROPYL ALCOHOL (UNII: 96F264O9SV) (Active Moiety)
Which are (fruli) Hand Antiseptic Rinse Free Gel 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- WATER (UNII: 059QF0KO0R)
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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".