FDA.reportPublic FDA data

Therabody Cleanse CBD Hand Sanitizer

Manufacturer
Theragun, Inc.
Effective date
2021-02-04
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:49:55

Label at a glance#

ProductTherabody Cleanse CBD Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Label contents#

Full prescribing information#

Active ingredient(s) Purpose

OTC - ACTIVE INGREDIENT SECTION

2oz Drug Panel2oz Drug Panel8oz drug panel8oz drug panel

Use(s)

OTC - PURPOSE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and

water are not available.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • on open skin wounds

When using this product

OTC - WHEN USING SECTION

  • keep out of eyes, ears, and mouth.
  • In case of contact with eyes,rinse eyes thoroughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation or rash occurs. These may be signs of serious condition.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact or contact a Poison Control Center right away.

Other information

STORAGE AND HANDLING SECTION

2oz Storage & Handling2oz Storage & Handling

When using this product

OTC - WHEN USING SECTION

  • Keep out of eyes, ears, and mouth.
  • in case of contact with eyes, rinse eyes thoroughly with water.

When using this product 8ozWhen using this product 8ozwhen using this product 2ozwhen using this product 2ozwhen using this product 2oz (2)when using this product 2oz (2)

INACTIVE INGREDIENT SECTION

InactiveInactive

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Cleanse 2oz MainCleanse 2oz MainCleanse 8floz MainCleanse 8floz Main

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81018-00281018-002-08
81018-00181018-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
HEMPTD1MUT01Q7IACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
XANTHAN GUMTTV12P4NEEIACT
ALCOHOL3K9958V90MACTIB
CLOVE OIL578389D6D0IACT
PEPPERMINT OILAV092KU4JHIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
XANTHAN GUMTTV12P4NEEIACT
HEMPTD1MUT01Q7IACT
ALCOHOL3K9958V90MACTIB
CLOVE OIL578389D6D0IACT
PEPPERMINT OILAV092KU4JHIACT

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
be24ba89-fcf4-98a2-e053-2995a90ad5aaba0c3b17-a12f-2b26-e053-2995a90a79eb2021-03-22WarningsExact identifier
spl set id: ba0c3b17-a12f-2b26-e053-2995a90a79eb

Reported adverse events (FAERS/openFDA)#

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