Fruit of the Earth

Manufacturer
Fruit Of The Earth, Inc.
Effective date
2021-08-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:38:28

Label at a glance#

ProductFruit of the Earth Acne Wash
Active ingredientSALICYLIC ACID
Label structure10 sections

Indications and uses

for the treatment of acne.

Dosage and administration

cover the entire affected area with a thin layer and rinse thoroughly one to three times daily because excessive drying of the skin may occur, start with one apllication daily, then gradually increase to two or three times daily if needed or as directed by a doctor if bothersome dryness or peeling occurs, reduce application to once a day or every other day.

Storage and handling

may stain some fabrics

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 2.0%

Purpose

OTC - PURPOSE SECTION

Acne Treatment

Uses

INDICATIONS & USAGE SECTION

for the treatment of acne.

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs only use one topical acne medication at a time.
  • avoid contact with eyes. If contact occurs, flush thoroughly with water.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • cover the entire affected area with a thin layer and rinse thoroughly one to three times daily
  • because excessive drying of the skin may occur, start with one apllication daily, then gradually increase to two or three times daily if needed or as directed by a doctor
  • if bothersome dryness or peeling occurs, reduce application to once a day or every other day.

Other information

STORAGE AND HANDLING SECTION

  • may stain some fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, sodium C14-16 olefin sulfonate, cocamidopropyl betaine, chamomilla recutita (matricaria) flower extract, cocamidopropyl PG-dimonium chloride phosphate, propylene glycol, aloe barbadensis leaf juice, anthemis nobilis flower extract, C12-15 alkyl lactate, PEG-80 sorbitan laurate, disodium EDTA, benzalkonium chloride, fragrance, yellow 5, red 40.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SP29001EFSP29001EF

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62217-93262217-932-87

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
24c845a2-a809-0b2d-e063-6394a90aa3ca935423fe-ae47-8b47-e053-2995a90ae2622024-10-18WarningsExact identifier
spl set id: 935423fe-ae47-8b47-e053-2995a90ae262

Reported adverse events (FAERS/openFDA)#

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