NDC 70889-800 Dr.bellca Hand Sanitizer Gel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70889 - Oneskin Cosmetics Co., Ltd.
- 70889-800 - Dr.bellca Hand Sanitizer Gel
Product Characteristics
Product Packages
NDC Code 70889-800-01
Package Description: 500 mL in 1 BOTTLE, PUMP
NDC Code 70889-800-02
Package Description: 236 mL in 1 BOTTLE, PUMP
NDC Code 70889-800-03
Package Description: 1 TUBE in 1 BOX / 50 mL in 1 TUBE
Product Details
What is NDC 70889-800?
What are the uses for Dr.bellca Hand Sanitizer Gel?
Which are Dr.bellca Hand Sanitizer Gel UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Dr.bellca Hand Sanitizer 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)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- EDETOL (UNII: Q4R969U9FR)
- ORANGE OIL (UNII: AKN3KSD11B)
- PEPPERMINT (UNII: V95R5KMY2B)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ALLANTOIN (UNII: 344S277G0Z)
- ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Dr.bellca Hand Sanitizer Gel?
- RxCUI: 581662 - ethanol 70 % Topical Gel
- RxCUI: 581662 - ethanol 0.7 ML/ML Topical Gel
- RxCUI: 581662 - ethyl alcohol 70 % Topical Gel
* Please review the disclaimer below.
[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".