Spread LOVE not Germs Rainbow Sprinkles Hand Sanitizer

Manufacturer
Base4 Ventures, LLC.
Effective date
2021-11-30
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:25:28

Label at a glance#

ProductSpread LOVE not Germs Rainbow Sprinkles Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

hand sanitizer to help decrease bacteria on the skin. recommended for repeated use.

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 66%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • hand sanitizer to help decrease bacteria on the skin.
  • recommended for repeated use.

Warnings

WARNINGS SECTION

  • For external use only.
  • Flammable.
  • Keep away from heat and flame.

Does not 

OTC - DO NOT USE SECTION

contain grain alcohol; do not drink. If taken internally will produce severe gastric disturbances

When using this product,

OTC - WHEN USING SECTION

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if redness or irritation develop and lasts.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a 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

  • Do not store above 105ºF.
  • may discolor some fabrics.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance, Water.

Package Labeling: Kit

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KitKit

Package Labeling:62651-032-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle5Bottle5

Package Labeling:62651-033-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle6Bottle6

Package Labeling:62651-034-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle7Bottle7

Package Labeling:62651-035-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle8Bottle8

Products#

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NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

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
086c5f26-a583-fef6-e063-6394a90a0175a9df8c10-59ac-d137-e053-2995a90ad00c2023-10-23WarningsExact identifier
spl set id: a9df8c10-59ac-d137-e053-2995a90ad00c

Reported adverse events (FAERS/openFDA)#

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