NDC 81227-000 Care Hand
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 81227-000-01
Package Description: 3785 mL in 1 BOTTLE
NDC Code 81227-000-02
Package Description: 59 mL in 1 BOTTLE
NDC Code 81227-000-03
Package Description: 118 mL in 1 BOTTLE
NDC Code 81227-000-04
Package Description: 237 mL in 1 BOTTLE
NDC Code 81227-000-05
Package Description: 296 mL in 1 BOTTLE
NDC Code 81227-000-06
Package Description: 473 mL in 1 BOTTLE
NDC Code 81227-000-07
Package Description: 946 mL in 1 BOTTLE
NDC Code 81227-000-08
Package Description: 1892.71 mL in 1 BOTTLE
NDC Code 81227-000-09
Package Description: 2 mL in 1 VIAL, SINGLE-USE
Product Details
What is NDC 81227-000?
What are the uses for Care Hand?
Which are Care Hand UNII Codes?
The UNII codes for the active ingredients in this product are:
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)
Which are Care Hand 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)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Care Hand?
- RxCUI: 581698 - isopropyl alcohol 70 % Topical Gel
- RxCUI: 581698 - isopropyl alcohol 0.7 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".