FDA.reportPublic FDA data

Sweet Grace Hand Sanitizer

Manufacturer
Bridgewater Candle Company LLC
Effective date
2023-11-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:21:19

Label at a glance#

ProductSweet Grace Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

Hand sanitizer to help decrease bacteria on  the skin

Dosage and administration

Wet hands thoroughly with product. Briskly rub hands together until dry. Supervise children in the use of this product.

Label contents#

Full prescribing information#

Active ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 65% v/v

OTC - PURPOSE SECTION

Antiseptic Hand Sanitizer

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help decrease bacteria on  the skin

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

in the eyes. In case of contact, flush eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if redness or irritation develop and persist for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, seek medical help or contact a Poison Control Center  immediately

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product.

  • Briskly rub hands together until dry.

  • Supervise children in the use of this product.

Other Information

OTHER SAFETY INFORMATION

  • store at 20°C to 25°C (68°F to 77°F)
  • may discolor certain fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Triethanolamine, Fragrance, Aloe Barbadensis Leaf  Juice, Tocopheryl Acetate

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

bottlebottle

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
81073-00081073-000-01

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
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
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
2cd80b76-788f-d75e-e063-6394a90af3b8b48e67e1-1459-423d-e053-2a95a90afc732025-01-29WarningsExact identifier
spl set id: b48e67e1-1459-423d-e053-2a95a90afc73

Reported adverse events (FAERS/openFDA)#

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