FDA.reportPublic FDA data

Epielle Exfoliating Scrub

Manufacturer
Kareway Product, Inc.
Effective date
2020-03-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:39:44

Label at a glance#

ProductEpielle Exfoliating Scrub Exfoliating Scrub
Active ingredientSALICYLIC ACID
Label structure10 sections

Storage and handling

Other information store at room temperature

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 2%

Purpose

OTC - PURPOSE SECTION

Acne treatment

INDICATIONS & USAGE SECTION

Use

penetrates pores to control acne blemishes and blackheads

WARNINGS SECTION

Warnings For external use only. Using other topical acne medication 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.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. If contact occurs, flush thoroughly with water.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

  • wet face
  • squeeze product into hands
  • massage over entire face
  • rinse thoroughly
  • for optimal results use 2-3 times per week

STORAGE AND HANDLING SECTION

Other information

store at room temperature

INACTIVE INGREDIENT SECTION

Inactive ingredients water, sodium cocoyl isethionate, glycerin, synthetic wax, glycol disearate, synthetic wax, stearyl alcohol, docamide MEA, PEG-6 caprylic/capric glycerides, sodium hydroxide, acrylates/c 10-30 alkyl acrylate crosspolymer, stearic acid, sodium benzoate, menthol, santhan gum, lavandula angustifolia(lavender) extract, salvia sclarea (clary) extract, hyacinthus orientalis (hyacinth) extract, chamomilla recutita (matricaria) flower/leaf extract, borago officinalis (borage) extract, centaurea cyanus (cornflower) flower extract, butylene glycol, 1,2-hexanediol, ethylhexylglyerin, blue 1 lake, fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Epielle exfoliating scrub

tubetube

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
67510-0403-52022-01-28C16284748780-19d75b9d0-7f15-f424-e053-dadaa90a57ceEpielle Exfoliating Scrub
67510-0403-52020-03-05C16284748780-19d75b9d0-7f15-f424-e053-dadaa90a57ceEpielle Exfoliating Scrub
67510-0403-52020-01-31C16284748780-19d75b9d0-7f15-f424-e053-dadaa90a57ceEpielle Exfoliating Scrub

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67510-040367510-0403-5

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
WATER059QF0KO0RIACT
SODIUM COCOYL ISETHIONATE518XTE8493IACT
GLYCERINPDC6A3C0OXIACT
STEARYL ALCOHOL2KR89I4H1YIACT
SYNTHETIC WAX (1200 MW)Q3Z4BCH099IACT
GLYCOL STEARATE0324G66D0EIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
COCAMIDE3YXD33R71GIACT
PEG-6 CAPRYLIC/CAPRIC GLYCERIDESGO50W2HWO8IACT
SODIUM HYDROXIDE55X04QC32IIACT
XANTHAN GUMTTV12P4NEEIACT
MENTHOLL7T10EIP3AIACT
SODIUM BENZOATEOJ245FE5EUIACT
SALICYLIC ACIDO414PZ4LPZACTIB

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
a020d17d-7b75-26bd-e053-2a95a90a67936d88a5ae-1608-c3d0-e053-2991aa0a39472020-03-05WarningsExact identifier
spl id: a020d17d-7b75-26bd-e053-2a95a90a6793
spl set id: 6d88a5ae-1608-c3d0-e053-2991aa0a3947

Reported adverse events (FAERS/openFDA)#

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