NDC 78565-005 Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 78565 - Meixin Beauty & Health Care Products Co., Ltd.
- 78565-005 - Hand Sanitizer
- 78565-005-02
- 78565-005-04
- 78565-005-05
- 78565-005-06
- 78565-005-07
- 78565-005-08
- 78565-005-12
- 78565-005-14
- 78565-005-15
- 78565-005-16
- 78565-005-17
- 78565-005-18
- 78565-005-24
- 78565-005-25
- 78565-005-34
- 78565-005-35
- 78565-005-44
- 78565-005-45
- 78565-005-54
- 78565-005-55
- 78565-005-64
- 78565-005-65
- 78565-005-75
- 78565-005-85
- 78565-005-95
- 78565-005 - Hand Sanitizer
Product Packages
NDC Code 78565-005-02
Package Description: 100 mL in 1 BOTTLE
NDC Code 78565-005-04
Package Description: 59 mL in 1 BOTTLE
NDC Code 78565-005-05
Package Description: 30 mL in 1 BOTTLE
NDC Code 78565-005-06
Package Description: 227 mL in 1 BOTTLE
NDC Code 78565-005-07
Package Description: 236 mL in 1 BOTTLE
NDC Code 78565-005-08
Package Description: 30 mL in 1 BOTTLE
NDC Code 78565-005-12
Package Description: 100 mL in 1 BOTTLE
NDC Code 78565-005-14
Package Description: 59 mL in 1 BOTTLE
NDC Code 78565-005-15
Package Description: 30 mL in 1 BOTTLE
NDC Code 78565-005-16
Package Description: 227 mL in 1 BOTTLE
NDC Code 78565-005-17
Package Description: 236 mL in 1 BOTTLE
NDC Code 78565-005-18
Package Description: 30 mL in 1 BOTTLE
NDC Code 78565-005-24
Package Description: 59 mL in 1 BOTTLE
NDC Code 78565-005-25
Package Description: 30 mL in 1 BOTTLE
NDC Code 78565-005-34
Package Description: 59 mL in 1 BOTTLE
NDC Code 78565-005-35
Package Description: 30 mL in 1 BOTTLE
NDC Code 78565-005-44
Package Description: 59 mL in 1 BOTTLE
NDC Code 78565-005-45
Package Description: 30 mL in 1 BOTTLE
NDC Code 78565-005-54
Package Description: 59 mL in 1 BOTTLE
NDC Code 78565-005-55
Package Description: 30 mL in 1 BOTTLE
NDC Code 78565-005-64
Package Description: 59 mL in 1 BOTTLE
NDC Code 78565-005-65
Package Description: 30 mL in 1 BOTTLE
NDC Code 78565-005-75
Package Description: 30 mL in 1 BOTTLE
NDC Code 78565-005-85
Package Description: 30 mL in 1 BOTTLE
NDC Code 78565-005-95
Package Description: 30 mL in 1 BOTTLE
Product Details
What is NDC 78565-005?
What are the uses for Hand Sanitizer?
Which are Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Hand Sanitizer 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:
- TROLAMINE (UNII: 9O3K93S3TK)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .ALPHA.-TOCOPHEROL SUCCINATE, D- (UNII: LU4B53JYVE)
- GLYCERIN (UNII: PDC6A3C0OX)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Hand Sanitizer?
- RxCUI: 1305100 - ethanol 75 % Topical Gel
- RxCUI: 1305100 - ethanol 0.75 ML/ML 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".