FDA.reportPublic FDA data

Sweet Shimmer SWEET POMEGRANATE Hand Sanitizer

Manufacturer
BASE4 Ventures, Inc
Effective date
2021-03-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:49:28

Label at a glance#

ProductSweet Shimmer SWEET POMEGRANATE Hand Sanitizer
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.66%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • For handwashing  to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire & flame.
Does not contain grain alcohol; do not drink. If taken internally will produce severe gastric disturbances.

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Condition worsens
  • Redness or irritation develops
  • 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 105°F
  • May discolor some fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Acrylate/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance, FD&C Red No. 4, D&C Red No. 33.

Questions?

OTC - QUESTIONS SECTION

Call 1-888-988-2427

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62651-05662651-056-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
FD&C RED NO. 4X3W0AM1JLXIACT
D&C RED NO. 339DBA0SBB0LIACT
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
c18301c4-e123-543b-e053-2a95a90ac13ebd087d25-0da9-e76a-e053-2995a90a48492021-05-04WarningsExact identifier
spl set id: bd087d25-0da9-e76a-e053-2995a90a4849

Reported adverse events (FAERS/openFDA)#

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