NDC 78445-101 Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 78445 - Guangzhou Kangfei Cosmetics Co., Ltd.
- 78445-101 - Hand Sanitizer
- 78445-101-01
- 78445-101-02
- 78445-101-03
- 78445-101-04
- 78445-101-05
- 78445-101-06
- 78445-101-07
- 78445-101-08
- 78445-101-09
- 78445-101-10
- 78445-101-11
- 78445-101-12
- 78445-101-13
- 78445-101-14
- 78445-101-15
- 78445-101-16
- 78445-101-17
- 78445-101-18
- 78445-101-19
- 78445-101-20
- 78445-101-21
- 78445-101-22
- 78445-101-23
- 78445-101-24
- 78445-101-25
- 78445-101-26
- 78445-101-27
- 78445-101-28
- 78445-101-29
- 78445-101-30
- 78445-101-31
- 78445-101-32
- 78445-101-33
- 78445-101-34
- 78445-101-35
- 78445-101-36
- 78445-101-37
- 78445-101-38
- 78445-101-39
- 78445-101-40
- 78445-101-41
- 78445-101-42
- 78445-101-43
- 78445-101-44
- 78445-101-45
- 78445-101 - Hand Sanitizer
Product Packages
NDC Code 78445-101-01
Package Description: 30 mL in 1 BOTTLE
NDC Code 78445-101-02
Package Description: 60 mL in 1 BOTTLE
NDC Code 78445-101-03
Package Description: 300 mL in 1 BOTTLE
NDC Code 78445-101-04
Package Description: 500 mL in 1 BOTTLE
NDC Code 78445-101-05
Package Description: 1000 mL in 1 BOTTLE
NDC Code 78445-101-06
Package Description: 2500 mL in 1 BOTTLE
NDC Code 78445-101-07
Package Description: 2.5 mL in 1 BOTTLE
NDC Code 78445-101-08
Package Description: 2000 mL in 1 BOTTLE
NDC Code 78445-101-09
Package Description: 2 mL in 1 BOTTLE
NDC Code 78445-101-10
Package Description: 3800 mL in 1 BOTTLE
NDC Code 78445-101-11
Package Description: 3000 mL in 1 BOTTLE
NDC Code 78445-101-12
Package Description: 3 mL in 1 BOTTLE
NDC Code 78445-101-13
Package Description: 4000 mL in 1 BOTTLE
NDC Code 78445-101-14
Package Description: 4 mL in 1 BOTTLE
NDC Code 78445-101-15
Package Description: 5000 mL in 1 BOTTLE
NDC Code 78445-101-16
Package Description: 5 mL in 1 BOTTLE
NDC Code 78445-101-17
Package Description: 6000 mL in 1 BOTTLE
NDC Code 78445-101-18
Package Description: 6 mL in 1 BOTTLE
NDC Code 78445-101-19
Package Description: 7600 mL in 1 BOTTLE
NDC Code 78445-101-20
Package Description: 8000 mL in 1 BOTTLE
NDC Code 78445-101-21
Package Description: 8 mL in 1 BOTTLE
NDC Code 78445-101-22
Package Description: 9 mL in 1 BOTTLE
NDC Code 78445-101-23
Package Description: 10000 mL in 1 BOTTLE
NDC Code 78445-101-24
Package Description: 10 mL in 1 BOTTLE
NDC Code 78445-101-25
Package Description: 15000 mL in 1 BOTTLE
NDC Code 78445-101-26
Package Description: 15 mL in 1 BOTTLE
NDC Code 78445-101-27
Package Description: 19000 mL in 1 BOTTLE
NDC Code 78445-101-28
Package Description: 20000 mL in 1 BOTTLE
NDC Code 78445-101-29
Package Description: 20 mL in 1 BOTTLE
NDC Code 78445-101-30
Package Description: 25000 mL in 1 BOTTLE
NDC Code 78445-101-31
Package Description: 38000 mL in 1 BOTTLE
NDC Code 78445-101-32
Package Description: 50 mL in 1 BOTTLE
NDC Code 78445-101-33
Package Description: 59 mL in 1 BOTTLE
NDC Code 78445-101-34
Package Description: 60 mL in 1 BOTTLE
NDC Code 78445-101-35
Package Description: 80 mL in 1 BOTTLE
NDC Code 78445-101-36
Package Description: 100 mL in 1 BOTTLE
NDC Code 78445-101-37
Package Description: 120 mL in 1 BOTTLE
NDC Code 78445-101-38
Package Description: 200 mL in 1 BOTTLE
NDC Code 78445-101-39
Package Description: 236 mL in 1 BOTTLE
NDC Code 78445-101-40
Package Description: 250 mL in 1 BOTTLE
NDC Code 78445-101-41
Package Description: 300 mL in 1 BOTTLE
NDC Code 78445-101-42
Package Description: 350 mL in 1 BOTTLE
NDC Code 78445-101-43
Package Description: 500 mL in 1 BOTTLE
NDC Code 78445-101-44
Package Description: 30 mL in 1 BOTTLE
NDC Code 78445-101-45
Package Description: 30 mL in 1 BOTTLE
Product Details
What is NDC 78445-101?
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:
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- TROLAMINE (UNII: 9O3K93S3TK)
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".