WEGMANS ALOE AFTER SUN GEL WITH LIDOCAINE HCL EXTERNAL ANALGESIC- lidocaine hydrochloride gel 
WEGMANS FOOD MARKETS INC

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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Wegmans Aloe After Sun Gel with Lidocaine HCl External Analgesic

Active ingredient

Lidocaine 0.8% (as Lidocaine HCI)

Purpose

External Analgesic

Uses

For the temporary relief of pain and itching associated with sunburn, minor burns, minor cuts, scrapes, insect bites, and minor skin irritations

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 eyes. If contact occurs, rinse with water to remove.

Stop use and ask a doctor if

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

Keep out of reach of children

If swallowed, seek medical help or contact a Poison Control Center immediately.

Directions

• Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily

• Children under 2 years of age: Ask a doctor.

Inactive ingredients

water, aloe barbadensis leaf juice, SD alcohol 40-B, laureth-23, polysorbate 20, glycerin, allantoin, carbomer, triethanolamine, menthyl lactate, menthol, fragrance, aleurites moluccanus seed extract, carica papaya (papaya) fruit extract, colocasia antiquorum root extract, mangifera indica (mango) fruit extract, passiflora incarnata flower extract, plumeria acutifolia flower extract, psidium guajava fruit extract, tocopheryl acetate (vitamin E acetate), tocopherol, phenoxyethanol, benzyl alcohol, fragrance

Label

WEG47651E3

WEGMANS ALOE AFTER SUN GEL WITH LIDOCAINE HCL EXTERNAL ANALGESIC 
lidocaine hydrochloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47124-129
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS8 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
MANGO (UNII: I629I3NR86)  
ALCOHOL (UNII: 3K9958V90M)  
LAURETH-23 (UNII: N72LMW566G)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
ALLANTOIN (UNII: 344S277G0Z)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
TROLAMINE (UNII: 9O3K93S3TK)  
MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)  
LEVOMENTHOL (UNII: BZ1R15MTK7)  
KUKUI NUT OIL (UNII: TP11QR7B8R)  
PAPAYA (UNII: KU94FIY6JB)  
COLOCASIA ESCULENTA ROOT (UNII: H7B71Q0G0D)  
PASSIFLORA INCARNATA FLOWER (UNII: K8F3G29S6Z)  
GUAVA (UNII: 74O70D6VG0)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
.ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
PLUMERIA ALBA FLOWER OIL (UNII: T69Z2432CU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47124-129-68454 g in 1 BOTTLE; Type 0: Not a Combination Product02/06/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34802/06/2019
Labeler - WEGMANS FOOD MARKETS INC (059650069)

Revised: 3/2023
Document Id: f70bc442-dd29-0a52-e053-6294a90a2b06
Set id: f70bc438-7ed8-f74d-e053-6394a90a2b3f
Version: 1
Effective Time: 20230316
 
WEGMANS FOOD MARKETS INC