NDC 75186-007 Primeauty Instant Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75186 - Huizhou Duomei Daily Necessites Co.,ltd
- 75186-007 - Primeauty Instant Hand Sanitizer
- 75186-007-01
- 75186-007-02
- 75186-007-03
- 75186-007-04
- 75186-007-05
- 75186-007-06
- 75186-007-07
- 75186-007-08
- 75186-007-09
- 75186-007-10
- 75186-007-11
- 75186-007-12
- 75186-007-13
- 75186-007-14
- 75186-007-15
- 75186-007-16
- 75186-007-17
- 75186-007-18
- 75186-007-19
- 75186-007-20
- 75186-007-21
- 75186-007-22
- 75186-007-23
- 75186-007-24
- 75186-007-25
- 75186-007-26
- 75186-007-27
- 75186-007-28
- 75186-007-29
- 75186-007-30
- 75186-007-31
- 75186-007-32
- 75186-007-33
- 75186-007 - Primeauty Instant Hand Sanitizer
Product Packages
NDC Code 75186-007-01
Package Description: 10 mL in 1 TUBE
NDC Code 75186-007-02
Package Description: 20 mL in 1 TUBE
NDC Code 75186-007-03
Package Description: 30 mL in 1 TUBE
NDC Code 75186-007-04
Package Description: 50 mL in 1 TUBE
NDC Code 75186-007-05
Package Description: 60 mL in 1 TUBE
NDC Code 75186-007-06
Package Description: 80 mL in 1 TUBE
NDC Code 75186-007-07
Package Description: 100 mL in 1 TUBE
NDC Code 75186-007-08
Package Description: 150 mL in 1 TUBE
NDC Code 75186-007-09
Package Description: 200 mL in 1 TUBE
NDC Code 75186-007-10
Package Description: 30 mL in 1 BOTTLE
NDC Code 75186-007-11
Package Description: 50 mL in 1 BOTTLE
NDC Code 75186-007-12
Package Description: 60 mL in 1 BOTTLE
NDC Code 75186-007-13
Package Description: 80 mL in 1 BOTTLE
NDC Code 75186-007-14
Package Description: 100 mL in 1 BOTTLE
NDC Code 75186-007-15
Package Description: 150 mL in 1 BOTTLE
NDC Code 75186-007-16
Package Description: 200 mL in 1 BOTTLE
NDC Code 75186-007-17
Package Description: 250 mL in 1 BOTTLE
NDC Code 75186-007-18
Package Description: 240 mL in 1 BOTTLE, PUMP
NDC Code 75186-007-19
Package Description: 250 mL in 1 BOTTLE, PUMP
NDC Code 75186-007-20
Package Description: 300 mL in 1 BOTTLE, PUMP
NDC Code 75186-007-21
Package Description: 350 mL in 1 BOTTLE, PUMP
NDC Code 75186-007-22
Package Description: 400 mL in 1 BOTTLE, PUMP
NDC Code 75186-007-23
Package Description: 500 mL in 1 BOTTLE, PUMP
NDC Code 75186-007-24
Package Description: 1000 mL in 1 BOTTLE, PUMP
NDC Code 75186-007-25
Package Description: 1000 mL in 1 DRUM
NDC Code 75186-007-26
Package Description: 2000 mL in 1 DRUM
NDC Code 75186-007-27
Package Description: 4000 mL in 1 DRUM
NDC Code 75186-007-28
Package Description: 5000 mL in 1 DRUM
NDC Code 75186-007-29
Package Description: 10000 mL in 1 DRUM
NDC Code 75186-007-30
Package Description: 15000 mL in 1 DRUM
NDC Code 75186-007-31
Package Description: 20000 mL in 1 DRUM
NDC Code 75186-007-32
Package Description: 25000 mL in 1 DRUM
NDC Code 75186-007-33
Package Description: 50000 mL in 1 DRUM
Product Details
What is NDC 75186-007?
What are the uses for Primeauty Instant Hand Sanitizer?
Which are Primeauty Instant 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 Primeauty Instant 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)
- TROLAMINE (UNII: 9O3K93S3TK)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- WATER (UNII: 059QF0KO0R)
- ALOE (UNII: V5VD430YW9)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
What is the NDC to RxNorm Crosswalk for Primeauty Instant 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".