EQUATE MOISTURIZING HAND SANITIZER WITH VITAMIN E

Manufacturer
Wal-Mart Stores, Inc.
Effective date
2020-04-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:05:26

Label at a glance#

ProductEQUATE MOISTURIZING HAND SANITIZER WITH VITAMIN E
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

Decreases bacteria on the skin that could cause disease recommended for repeated use

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping for children under 6, use only under adult supervision not recommended for infants

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 65%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • Decreases bacteria on the skin that could cause disease
  • recommended for repeated use

WARNINGS

WARNINGS SECTION

For external use only: hands
Flammable, keep away from fire or flame.
When using this product
• keep out of eyes. In case of contact with eyes flush thoroughly with water.
• avoid contact with broken skin
• do not inhale or ingest

Stop use and ask doctor if

  • irritation and redness develop
  • condition persists for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands thoroughly with product and allow to dry without wiping
  • for children under 6, use only under adult supervision
  • not recommended for infants

Other information

OTHER SAFETY INFORMATION

  • not store above 105°F
  • may discolor some fabrics
  • harmful to wood finishes and plastics

Inactive ingredient

INACTIVE INGREDIENT SECTION

water, glycerin, acrylates/c10-30 alkyl acrylate crosspolymer, triethanolamine, fragrance, tocopheryl acetate, panthenol

Questions?

OTC - QUESTIONS SECTION

1-888-287-1915

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EQT_12oz_Orig_GelHandSanitizer_V2EQT_12oz_Orig_GelHandSanitizer_V2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
902574ethanol 65 % Topical GelPSN3
902574ethanol 0.65 ML/ML Topical GelSCD3
902574ethyl alcohol 65 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49035-557-03EQUATE MOISTURIZING HAND SANITIZER WITH VITAMIN E89 mL in 1 BOTTLEGEL893
49035-557-12EQUATE MOISTURIZING HAND SANITIZER WITH VITAMIN E355 mL in 1 BOTTLEGEL3553
49035-557-34EQUATE MOISTURIZING HAND SANITIZER WITH VITAMIN E1000 mL in 1 BOTTLEGEL10003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49035-557EQUATE MOISTURIZING HAND SANITIZER WITH VITAMIN E (ETHYL ALCOHOL) GEL [WAL-MART STORES, INC.]3Legacy NDC, 3 package rows20200408_e7aefe7a-327b-4475-a152-58fbba8f0f34.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49035-55749035-557-03, 49035-557-12, 49035-557-34

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML · Source PDF

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
a8f50359-a008-41f1-a6b9-13d72f7c1d6de7aefe7a-327b-4475-a152-58fbba8f0f342020-04-07WarningsExact identifier
spl id: a8f50359-a008-41f1-a6b9-13d72f7c1d6d
spl set id: e7aefe7a-327b-4475-a152-58fbba8f0f34

Reported adverse events (FAERS/openFDA)#

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