FDA.reportPublic FDA data

Hand Sanitizer Spray Pen Whipped Vanilla spray

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 22:25:31

Label at a glance#

ProductHand Sanitizer Pen Whipped Vanilla
Active ingredientALCOHOL
Label structure8 sections

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. 70%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

  • To decrease bacteria on the skin.

Warnings

WARNINGS SECTION

  • For external use only.
  • Flammable, keep away from heat and flame
  • Does not contain grain alcohol; do not drink. If taken internally will produce serious gastric disturbances

When using this product

OTC - WHEN USING SECTION

  • Avoid the eyes and mucous membranes
  • In the case of eyes or mucous membrane contact, rinse thoroughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Condition worsens
  • Redness or irritation develops
  • If condition persists for more than 3 days

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed contact a doctor or 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

  • Store below 105ºF
  • May discolor some fabrics

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Water, Glycerin, F ragrance, Disodium EDTA.

Questions?

OTC - QUESTIONS SECTION

Call 1-888-988-2427

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label9Label9

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
62651-06162651-061-01

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
GLYCERINPDC6A3C0OXIACT
DISODIUM EDTA-COPPER6V475AX06UIACT
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
086c92a9-2e28-a240-e063-6394a90a5089c134d931-fda7-8fd9-e053-2a95a90abecf2023-10-23WarningsExact identifier
spl set id: c134d931-fda7-8fd9-e053-2a95a90abecf

Reported adverse events (FAERS/openFDA)#

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