ALOE VERA GEL- lidocaine hcl, menthol gel 
Retail Business Services, LLC

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

Do not use

in large quantities, particularly over raw surfaces or blistered areas

When using this product

avoid contact with the eyes

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:

AUDSA DISTRIBUTION, LLC

SALISBURY, NC 28147

For product questions or concerns, contact us at 1-833-992-3872

Quality guaranteed or your money back.

DSP-TN-21091

DSP-MO-20087

principal display panel

CAREONE

AFTER SUN

Gel with Aloe

Pain Relieving Gel

NET 16 FL OZ (473 mL)

image description

ALOE VERA GEL 
lidocaine hcl, menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72476-747
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)  
CARBOXYPOLYMETHYLENE (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:72476-747-43473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/24/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34811/24/2021
Labeler - Retail Business Services, LLC (967989935)
Registrant - Vi-Jon, LLC (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC790752542manufacture(72476-747)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC088520668manufacture(72476-747)

Revised: 1/2023
Document Id: c490f5f8-1f7c-45af-b022-1d85010be8fd
Set id: 073c72fe-3171-4a4f-913a-d1b9630a1af3
Version: 4
Effective Time: 20230109
 
Retail Business Services, LLC