FDA.reportPublic FDA data

Mint

Manufacturer
Brands International Corp
Effective date
2020-04-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:36:37

Label at a glance#

ProductMint
Active ingredientALCOHOL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient - Ethanol 62%

OTC - PURPOSE SECTION

Purpose - Antiseptic

INDICATIONS & USAGE SECTION

Use

  • to decrease bacteria on the skin and clean hands
  • recommeded for repeated use

WARNINGS SECTION

Warnings

for external use only

Flammable, keep away from fire or flame

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of children. If accidently swallowed, get medical helpor contact a Poison Control Center right away

USER SAFETY WARNINGS SECTION

Do not get into eyes, If contact occurs, rinse thoroughly with water

OTC - ASK DOCTOR/PHARMACIST SECTION

Discontinue Use if irritation or redness develops, If irritation persists for more than 72 hours, consult a doctor

DOSAGE & ADMINISTRATION SECTION

Directions

  • apply to hands until thoroughly wet
  • rub vigorously until dry
  • supervise children in the use of this product

USER SAFETY WARNINGS SECTION

Other information

  • may discolor certain fabrics or surfaces
  • do not store above 110 F (43 C)

INACTIVE INGREDIENT SECTION

Purified water, Peppermint Essential Oil, Spearmint Essential Oil, Lemongrass Essential Oil, Vegetable Glycerin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

UntitledUntitled

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
50157-30050157-300-60

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
GLYCERINPDC6A3C0OXIACT
PEPPERMINT OILAV092KU4JHIACT
SPEARMINT OILC3M81465G5IACT
EAST INDIAN LEMONGRASS OILUP0M8M3VZWIACT
WATER059QF0KO0RIACT
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
a342d6cf-396c-307e-e053-2a95a90a287e0752d8bd-80ce-4c08-a334-3a747dbd86142020-04-14WarningsExact identifier
spl set id: 0752d8bd-80ce-4c08-a334-3a747dbd8614

Reported adverse events (FAERS/openFDA)#

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