FDA.reportPublic FDA data

Hand Sanitizer Sling Sweet Melon

Manufacturer
BASE4 Ventures, Inc
Effective date
2021-04-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:45:35

Label at a glance#

ProductHand Sanitizer Sling Sweet Melon
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

hand sanitizer to help decrease bacteria on the skin. recommended for repeated use.

Dosage and administration

Rub dime sized amount between hands until dry. Supervise children in the use of this product. In the case of eye contact rinse eyes thoroughly with water

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol Denat. 66% (V/V)

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • hand sanitizer to help decrease bacteria on the skin.
  • recommended for repeated use.

Warnings

WARNINGS SECTION

  • For external use only.
  • Flammable. 
  • Keep away from heat or flame. 
  • Does not contain grain alcohol; do not drink. If taken internally will produce severe gastric disturbances.

When using this product, 

OTC - WHEN USING SECTION

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if redness or irritation develop and lasts.

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Rub dime sized amount between hands until dry.
  • Supervise children in the use of this product. In the case of eye contact rinse eyes thoroughly with water

Other information

SPL UNCLASSIFIED SECTION

  • Do not store above 105°F.
  • May discolor some fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acrylates/C10-30 alkyl acrylates crosspolymer, Aminomethyl propanol, D&C Red No.33, Disodium EDTA, FD&C Blue No.1, FD&C Red No.4, FD&C Yellow No.5, Fragrance, Water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SM_29SM_29

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62651-04262651-042-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
D&C RED NO. 339DBA0SBB0LIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C RED NO. 4X3W0AM1JLXIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
c1359f65-3977-ca29-e053-2a95a90a0e53b48c6754-e967-52cf-e053-2995a90ad9ab2021-04-30WarningsExact identifier
spl id: c1359f65-3977-ca29-e053-2a95a90a0e53
spl set id: b48c6754-e967-52cf-e053-2995a90ad9ab

Reported adverse events (FAERS/openFDA)#

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