Get-Gone - Acne Body Cleanser

Manufacturer
Maelys Cosmetics, LTD
Effective date
2025-06-04
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 20:37:20

Label at a glance#

ProductGet-Gone - Acne Body Cleanser
Active ingredientSALICYLIC ACID
Label structure8 sections

Indications and uses

• For the treatment of acne

Dosage and administration

• In the shower, lather with water. • Massage all over wet skin, paying special attention to areas with acne. • Rinse thoroughly.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 2%

Purpose

OTC - PURPOSE SECTION

Acne treatment

Uses

INDICATIONS & USAGE SECTION

• For the treatment of acne

Warnings

WARNINGS SECTION

For external use only.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor. • Do not get into eyes. tt excessive skin irritation develops or increases, discontinue use and consult a doctor. • If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• In the shower, lather with water. • Massage all over wet skin, paying special attention to areas with acne. • Rinse thoroughly.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, Decyl Glucoside, Lauryl Glucoside, Sodium Cocoyl isethionate, Cocamidopropyl Betaine, PEG-150 Distearate, Sodium Cocoamphoacetate, Panthenol, Hamamelis Virginiana (Witch Hazel) Leaf Extract, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Salix Alba (Willow) Bark Extract, pilobium Fleischeri Flower/Leaf/Stem Extract, Chamomilla Recutita (Matricaria) Flower Extract, Lavandula Angustifolia (Lavender) Oil, Mentha Piperita (Peppermint) Leaf Oil, Glycerin, Coconut Acid, Sodium Chloride, Sodium Cocoyl Glutamate, Sodium Lauryl Glucose Carboxylate, Parfum (Fragrance), Chlorphenesin, Disodium EDTA, Phenoxyelhanol, Citric Acid.

Other Information

SPL UNCLASSIFIED SECTION

Protect this product from excessive heat and direct sun.

Question or Comments:

OTC - QUESTIONS SECTION

1-800-253-1983

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

011011

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83010-01183010-011-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 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
36b89e2e-4b20-67df-e063-6294a90ae26de4ff846b-2c25-40cb-a669-50dd9338d3c92025-06-04WarningsExact identifier
spl id: 36b89e2e-4b20-67df-e063-6294a90ae26d
spl set id: e4ff846b-2c25-40cb-a669-50dd9338d3c9

Reported adverse events (FAERS/openFDA)#

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