SunDrops 71

Manufacturer
Sunburst Chemicals, Inc.
Effective date
2022-12-07
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:45:23

Label at a glance#

ProductSunDrops 71
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Dispense a small amount of spray onto the hands. Spread on hands and rub into skin until dry. Dispense a smaller amount in one hand and spread over both hands and wrists. Rub into skin until dry. Children should be supervised while using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 60%

​Purpose

OTC - PURPOSE SECTION

Skin Sanitizer

​Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce the amount of bacteria on the skin

​Warnings

WARNINGS SECTION

Flammable.  Keep away from fire or flame.

For external use only.  If swallowed, seek medical attention.

When using this product do not use around or near the eyes.  If contact occurs, flush eyes with water and contact doctor immediately.

Stop use and consult a doctor when skin irritation appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

​Directions

DOSAGE & ADMINISTRATION SECTION

  • Dispense a small amount of spray onto the hands.
  • Spread on hands and rub into skin until dry.
  • Dispense a smaller amount in one hand and spread over both hands and wrists.
  • Rub into skin until dry.
  • Children should be supervised while using this product.

​Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Propylene Glycol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Case Label - 8 x 1000 mL BagsCase Label - 8 x 1000 mL Bags

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
63621-37163621-371-20

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
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT

Source Document#

Source XML · Source PDF

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
0a4ad9ab-a3bc-07ba-e063-6394a90a2453bf55f46f-2e48-4d84-a8e2-0c5b15694a2d2023-11-16WarningsExact identifier
spl set id: bf55f46f-2e48-4d84-a8e2-0c5b15694a2d

Reported adverse events (FAERS/openFDA)#

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