FDA.reportPublic FDA data

Hand Sanitizer Sling Winter Berry

Manufacturer
Base4 Ventures, LLC. | Ganzhou Olivee Cosmetic Co., Ltd.
Effective date
2021-11-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:25:30

Label at a glance#

ProductHand Sanitizer Sling Winter Berry
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 Ingredients

OTC - ACTIVE INGREDIENT SECTION

Alcohol Denat 66%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

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 and flame.

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 105ºF.
  • may discolor some fabrics.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Water, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62651-05862651-058-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
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
086c76d7-ec1d-6051-e063-6294a90a3695c134c327-9dc4-2df0-e053-2995a90afbc62023-10-23WarningsExact identifier
spl set id: c134c327-9dc4-2df0-e053-2995a90afbc6

Reported adverse events (FAERS/openFDA)#

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