ANDYS BEST- alcohol gel 
Brand Name Distributors

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Active Ingredient(s)

ActiveAlcohol 70% v/v. Purpose: Antimicrobial

Purpose

  1. Antimicrobial
    purpose
    , Hand Sanitizer

Use

indicatiHand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WarningFor external use only. Flammable. Keep away from heat or flame

Do not use

do not

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

when

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

KeepKeep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

dosage

Other information

storage

Inactive ingredients


WATER, CARBOMER, inactive TRIETHANOLAMINE LAURYL SULFATE

Package Label - Principal Display Panel

ADVANCED HAND SANITIZER

ANTIMICROBIAL

33.8 FL OZ (1L)

PRINCIPAL

ANDYS BEST 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73755-120
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CARBOMER 1342 (UNII: 809Y72KV36) 0.0025 mL  in 1 mL
TRIETHANOLAMINE LAURYL SULFATE (UNII: E8458C1KAA) 0.004 mL  in 1 mL
WATER (UNII: 059QF0KO0R) 0.29 mL  in 1 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73755-120-041000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/30/2020
Labeler - Brand Name Distributors (078570365)

Revised: 5/2020
Document Id: a4f2b5db-ec5a-705f-e053-2995a90a678d
Set id: a4f332d7-0942-4bbc-e053-2995a90ae5c6
Version: 1
Effective Time: 20200505
 
Brand Name Distributors