ALOE VERA GEL- lidocaine hcl, menthol gel 
Amazon

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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After Sun Gel with Aloe
747.001/747AB

Active ingredient

Lidocaine HCl 0.7%

Menthol 0.2%

Purpose

topical analgesic

Uses

for the temporary relief of pain and itching associated with

Warnings

For external use only

When using this product

avoid contact with the eyes

do not use

in large quantities, particularly over raw surfaces or blistered areas

Stop use and ask a doctor if

condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away

Directions

inactive ingredients

water, alcohol denat., polysorbate 20, glycerin, Aloe barbadensis leaf juice, carbomer, benzophenone-4, triethanolamine, benzyl alcohol, phenoxyethanol, blue 1

DISTRIBUTED BY:

Amazon.com Services, Inc.

Seattle, WA 98109 

1-877-485-0385

@2022 Amazon.com, Inc. or its

affiliates. All rights reserved. 

www.amazon.com/amazonbasics

DSP-TN-21091

DSP-MO-20087

"Alexa, reorder Amazon Basics After Sun Gerl." alexa

principal display panel

amazon basics

After Sun Gel

With Aloe

Pain Relieveing Gel

with Aloe Vera, Lidocaine & Menthol

16 FL OZ (473 mL)

image description

ALOE VERA GEL 
lidocaine hcl, menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72288-747
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS7 mg  in 1 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL2 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
water (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
SULISOBENZONE (UNII: 1W6L629B4K)  
TROLAMINE (UNII: 9O3K93S3TK)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72288-747-43473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/17/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34805/17/2018
Labeler - Amazon (128990418)
Registrant - Vi-Jon, LLC (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC790752542manufacture(72288-747)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC088520668manufacture(72288-747)

Revised: 9/2023
Document Id: a6fa6101-2e01-40be-8d85-4cf03d122ce8
Set id: 2acb1a6a-57e6-4915-b03a-89d1d2db3baf
Version: 12
Effective Time: 20230911
 
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