NDC 81410-102 Aim-x Antibacterial Hand Cleansing Gel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 81410 - Aim-x Global, Too.
- 81410-102 - Aim-x Antibacterial Hand Cleansing Gel
- 81410-102-01
- 81410-102-02
- 81410-102-03
- 81410-102-04
- 81410-102-05
- 81410-102-06
- 81410-102-07
- 81410-102-08
- 81410-102-09
- 81410-102-10
- 81410-102-11
- 81410-102-12
- 81410-102-13
- 81410-102-14
- 81410-102-15
- 81410-102-16
- 81410-102-17
- 81410-102-18
- 81410-102-19
- 81410-102-20
- 81410-102-21
- 81410-102-22
- 81410-102-23
- 81410-102-24
- 81410-102-25
- 81410-102-26
- 81410-102-27
- 81410-102-28
- 81410-102 - Aim-x Antibacterial Hand Cleansing Gel
Product Packages
NDC Code 81410-102-01
Package Description: 5 mL in 1 BOTTLE
NDC Code 81410-102-02
Package Description: 7 mL in 1 BOTTLE
NDC Code 81410-102-03
Package Description: 10 mL in 1 BOTTLE
NDC Code 81410-102-04
Package Description: 20 mL in 1 BOTTLE
NDC Code 81410-102-05
Package Description: 30 mL in 1 BOTTLE
NDC Code 81410-102-06
Package Description: 50 mL in 1 BOTTLE
NDC Code 81410-102-07
Package Description: 75 mL in 1 BOTTLE
NDC Code 81410-102-08
Package Description: 100 mL in 1 BOTTLE
NDC Code 81410-102-09
Package Description: 120 mL in 1 BOTTLE
NDC Code 81410-102-10
Package Description: 150 mL in 1 BOTTLE
NDC Code 81410-102-11
Package Description: 200 mL in 1 BOTTLE
NDC Code 81410-102-12
Package Description: 250 mL in 1 BOTTLE
NDC Code 81410-102-13
Package Description: 300 mL in 1 BOTTLE
NDC Code 81410-102-14
Package Description: 400 mL in 1 BOTTLE
NDC Code 81410-102-15
Package Description: 500 mL in 1 BOTTLE
NDC Code 81410-102-16
Package Description: 650 mL in 1 BOTTLE
NDC Code 81410-102-17
Package Description: 750 mL in 1 BOTTLE
NDC Code 81410-102-18
Package Description: 900 mL in 1 BOTTLE
NDC Code 81410-102-19
Package Description: 1000 mL in 1 BOTTLE
NDC Code 81410-102-20
Package Description: 1250 mL in 1 BOTTLE
NDC Code 81410-102-21
Package Description: 1500 mL in 1 BOTTLE
NDC Code 81410-102-22
Package Description: 2000 mL in 1 BOTTLE
NDC Code 81410-102-23
Package Description: 2500 mL in 1 BOTTLE
NDC Code 81410-102-24
Package Description: 5000 mL in 1 CAN
NDC Code 81410-102-25
Package Description: 10000 mL in 1 CAN
NDC Code 81410-102-26
Package Description: 15000 mL in 1 CAN
NDC Code 81410-102-27
Package Description: 20000 mL in 1 CAN
NDC Code 81410-102-28
Package Description: 30000 mL in 1 CAN
Product Details
What is NDC 81410-102?
What are the uses for Aim-x Antibacterial Hand Cleansing Gel?
Which are Aim-x Antibacterial Hand Cleansing Gel 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 Aim-x Antibacterial Hand Cleansing 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:
- WATER (UNII: 059QF0KO0R)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- GLYCERIN (UNII: PDC6A3C0OX)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- TROLAMINE (UNII: 9O3K93S3TK)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
What is the NDC to RxNorm Crosswalk for Aim-x Antibacterial Hand Cleansing Gel?
- RxCUI: 581698 - isopropyl alcohol 70 % Topical Gel
- RxCUI: 581698 - isopropyl alcohol 0.7 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".