FDA.reportPublic FDA data

Aloe Vera Gel

Manufacturer
Walmart Inc. | Nice-Pak Products, LLC
Effective date
2026-02-27
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:47:37

Label at a glance#

ProductAloe Vera Gel
Active ingredientLIDOCAINE HYDROCHLORIDE, MENTHOL
Label structure13 sections

Indications and uses

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

Dosage and administration

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

Label contents#

Full prescribing information#

Claims

SPL UNCLASSIFIED SECTION

with Aloe

Sunburn relief Gel

Sunburn Relief Gel with Aloe helps relieve the pain of irritated, sunburned skin. Medicated sunburn relief moisturizes skin on contact to help support skin's natural moisture balance. Lidocaine and menthol help bring fast relief to different skin irratations, like sunburn, minor burns, minor cuts, scrapes, insect bites and windburn.

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine HCl 0.7%
Menthol 0.2%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Uses

INDICATIONS & USAGE SECTION

for the temporary relief of pain and itching associated with

  • minor burns 
  • sunburn 
  • minor cuts 
  • scrapes 
  • insect bites
  • minor skin irritations

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

in large quantities, particularly over raw surfaces or blistered areas

When using this product

OTC - WHEN USING SECTION

avoid contact with the eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

INACTIVE INGREDIENT SECTION

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

ADVERSE REACTION

ADVERSE REACTIONS SECTION

DSP-TN-21091 DSP-MO-20087

Satisfaction guaranteed

For more information call 1-888-287-1915 or visit Walmart.com/help

DISTRIBUTED BY: Walmart Inc.,

Bentonville, AR 72716

Made in the USA with domestic and imported ingredients

Factory Certifited

Empty Before Recycling

PLASTIC BOTTLE

how2recycle.info

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 79903-352-20

equate™

Sunburn relief

Gel

with Aloe

AFTER SUN

with Lidocaine HCL and Menthol

  • Sunburn pain relief

PARABEN FREE

20 FL OZ (1 PT 4 FL OZ) 591 mL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1361205lidocaine HCl 0.7 % / menthol 0.2 % Topical GelPSN3
1361205lidocaine hydrochloride 0.007 MG/MG / menthol 0.002 MG/MG Topical GelSCD3
1361205lidocaine hydrochloride 0.7 % / menthol 0.2 % Topical GelSY3

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79903-352-20Aloe Vera Gel591 mL in 1 BOTTLE, PLASTICGEL5913

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79903-35279903-352-20

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
POLYSORBATE 207T1F30V5YHIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAF JUICERUE8E6T4NBIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
SULISOBENZONE1W6L629B4KIACT
SODIUM HYDROXIDE55X04QC32IIACT
BENZYL ALCOHOLLKG8494WBHIACT
PHENOXYETHANOLHIE492ZZ3TIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
LIDOCAINE HYDROCHLORIDEV13007Z41AACTIR
MENTHOLL7T10EIP3AACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Aloe Vera GelLIDOCAINE HCL, MENTHOLWalmart Inc.309dcf5b-7166-976a-e063-6394a90af9522026-02-27Warnings, Adverse reactionsExact identifier
ndc (package): 79903-352-20
ndc (product): 79903-352
ndc11 (package): 79903035220
spl id: 4bd51bda-1e8a-2381-e063-6294a90aea5b
spl set id: 309dcf5b-7166-976a-e063-6394a90af952

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.