FDA.reportPublic FDA data

Symmetry Foaming Hand Sanitizer

Manufacturer
Buckeye International, Inc.
Effective date
2025-03-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:57:59

Label at a glance#

ProductSymmetry Foaming Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin that could cause disease Recommended for repeated use

Dosage and administration

Dispense an adequate amount of hand sanitizer Rub Hands together until completely dry

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antibacterial

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external uses only.

OTC - WHEN USING SECTION

When using this product do not use in or near eyes.

If in eyes, flush thoroughly with water.

OTC - STOP USE SECTION

If irritation or rash appears and persists, stop use and see a physician.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, call a physician or Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Dispense an adequate amount of hand sanitizer
  • Rub Hands together until completely dry

Other information

OTHER SAFETY INFORMATION

  • Do not store above 110°F (43°C)
  • May discolor some fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), PEG-10 Dimethicone, PEG-12 Dimethicone, PEG-8 Dimethicone, Glycerine, Propylene Glycol, Isopropyl Myristate, Fragrance (Parfum). Aloe Barbadensis Leaf Juice, and Tocopheryl Acetate.

Questions?

OTC - QUESTIONS SECTION

Call: Buckeye International, Inc. • 314-291-1900

Monday through Friday • 8:00 a.m. to 5:00 p. m. CST

Uses

INDICATIONS & USAGE SECTION

  • Hand sanitizer to help reduce bacteria on the skin that could cause disease
  • Recommended for repeated use

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

symmetry

FOAMING HAND

SANITIZER

w/ Aloe &Vitamin E

Made in USA

LP Product # 9005300

NET CONTENTS 1000 ml (33.8 fl oz)

container labelBcontainer labelB

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
616805ethanol 70 % Topical FoamPSN1
616805ethanol 0.7 ML/ML Topical FoamSCD1
616805ethanol 70 % Topical FoamSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
30805-021-09Symmetry Foaming Hand Sanitizer1000 mL in 1 BAGLIQUID10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
30805-021SYMMETRY FOAMING HAND SANITIZER (ALCOHOL) LIQUID [BUCKEYE INTERNATIONAL, INC.]1Current NDC, 1 package rows20250330_1cfcad5c-3896-3f69-e063-6294a90a8d9e.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
30805-02130805-021-09

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
PEG-10 DIMETHICONE (600 CST)8PR7V1SVM0IACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
ALOEV5VD430YW9IACT
PEG-8 DIMETHICONEGIA7T764ODIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PEG-12 DIMETHICONE (300 CST)ZEL54N6W95IACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
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
Symmetry Foaming Hand SanitizerALCOHOLBuckeye International, Inc.1cfcad5c-3896-3f69-e063-6294a90a8d9e2025-03-27WarningsExact identifier
ndc (package): 30805-021-09
ndc (product): 30805-021
ndc11 (package): 30805002109
spl id: 1cfcad5c-3897-3f69-e063-6294a90a8d9e
spl set id: 1cfcad5c-3896-3f69-e063-6294a90a8d9e

Reported adverse events (FAERS/openFDA)#

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