FDA.reportPublic FDA data

Hand Sanitizer Spray Sweet Pomegranate

Manufacturer
BASE4 Ventures, Inc
Effective date
2021-02-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:53:43

Label at a glance#

ProductHand Sanitizer Sweet Pomegranate
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

For hand washing to decrease bacteria on the skin

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 62%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • For hand washing 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, Carbomer, Propylene Glycol, Fragrance, Triethanolamine, Tocopheryl Acetate, Aloe Barbadensis Extract, Dimethicone.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SpraySpray

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62651-02762651-027-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
DIMETHICONE92RU3N3Y1OIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
TROLAMINE9O3K93S3TKIACT

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
bafb21d2-ec05-7029-e053-2995a90a399eaaf5a5f2-f885-144f-e053-2995a90a30c12021-02-10WarningsExact identifier
spl id: bafb21d2-ec05-7029-e053-2995a90a399e
spl set id: aaf5a5f2-f885-144f-e053-2995a90a30c1

Reported adverse events (FAERS/openFDA)#

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