FDA.reportPublic FDA data

Deep Pore Acne Scrub

Manufacturer
derma e | Topiderm, Inc.
Effective date
2018-11-08
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:04:52

Label at a glance#

ProductDeep Pore Acne Scrub
Active ingredientSALICYLIC ACID
Label structure9 sections

Indications and uses

For the treatment of acne

Dosage and administration

Apply a small amount to wet skin. Cover the entire affected area with a thin layer, gently massage in circular motion. Rinse thoroughly with warm water and pat dry. Because excessive drying of the skin may occur, start with one application 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 eve...

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

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

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply a small amount to wet skin.
  • Cover the entire affected area with a thin layer, gently massage in circular motion. Rinse thoroughly with warm water and pat dry.
  • Because excessive drying of the skin may occur, start with one application 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.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Cetyl Alcohol (Plant Derived), Prunus Armeniaca (Apricot) Seed Powder, Stearic Acid (Vegetable Derived), Glyceryl Stearate Citrate (Vegetable Derived), Hydroxypropyl Starch Phosphate (Sugar Starch), Caprylic/Capric Triglyceride (Vegetable Derived), Glycerin (Vegetable Derived), Decyl Glucoside (Plant Derived), Xanthan Gum, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Lavandula Angustifolia (Lavender) Oil, Aniba Rosodora (Rosewood) Wood Oil, Salix Alba (Willow) Bark Extract, Allantoin, Organic Aloe Barbadensis (Aloe Vera) Extract1, Organic Simmondsia Chinensis (Jojoba) Seed Oil1, Organic Chamomilla Recutita (Matricaria) Flower Extract1, Polysorbate 60, Polysorbate 20, Glyceryl Stearate SE, Potassium Sorbate, Phenoxyethanol, Ethylhexylglycerin.

SPL UNCLASSIFIED SECTION

Distributed by DERMA E®
Simi Valley, CA 93065, USA

PRINCIPAL DISPLAY PANEL - 113 g Tube Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ANTI-ACNE

100% VEGAN • GMO-FREE
ECO-ETHICAL
CRUELTY-FREE

DERMA•E

Deep Pore
Acne Scrub

Active Salicylic Acid
with Tea Tree Oil + Aloe Vera

4 OZ / 113 g

PRINCIPAL DISPLAY PANEL - 113 g Tube Label
PRINCIPAL DISPLAY PANEL - 113 g Tube Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
562600salicylic acid 2 % Medicated Liquid SoapPSN5
562600salicylic acid 20 MG/ML Medicated Liquid SoapSCD5
562600salicylic acid 2 % Facial Cleanser TonerSY5
562600salicylic acid 2 % Facial ScrubSY5
562600salicylic acid 2 % Medicated Liquid SoapSY5

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54108-3750-12025-01-30C16284748780-12cef2736-7da4-d83d-e063-dadaa90ab31fDeep Pore Acne Scrub

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54108-3750-1Deep Pore Acne Scrub113 g in 1 TUBEPASTE1135

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54108-3750DEEP PORE ACNE SCRUB (SALICYLIC ACID) PASTE [DERMA E]5Legacy NDC, 1 package rows20231219_b210f5da-d4d9-49dd-8947-220040ab32e1.zip

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54108-375054108-3750-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB
WATER059QF0KO0RIACT
PRUNUS ARMENIACA SEED75356789IWIACT
CETYL ALCOHOL936JST6JCNIACT
GLYCERYL STEARATE CITRATEWH8T92A065IACT
HYDROXYPROPYL DISTARCH PHOSPHATE, HIGH AMYLOSE CORN9F8ET54T05IACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
GLYCERINPDC6A3C0OXIACT
STEARIC ACID4ELV7Z65APIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
TEA TREE OILVIF565UC2GIACT
LAVENDER OILZBP1YXW0H8IACT
ALLANTOIN344S277G0ZIACT
SALIX ALBA BARK205MXS71H7IACT
ROSEWOOD OILF2522O5L7BIACT
JOJOBA OIL724GKU717MIACT
MATRICARIA CHAMOMILLA WHOLEG0R4UBI2ZZIACT
ALOE VERA LEAFZY81Z83H0XIACT
XANTHAN GUMTTV12P4NEEIACT
POLYSORBATE 207T1F30V5YHIACT
POLYSORBATE 60CAL22UVI4MIACT
GLYCERYL STEARATE SEFCZ5MH785IIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
PHENOXYETHANOLHIE492ZZ3TIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT

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
1a5725d8-9f67-45d8-a126-73116f794ec5b210f5da-d4d9-49dd-8947-220040ab32e12018-11-08WarningsExact identifier
spl id: 1a5725d8-9f67-45d8-a126-73116f794ec5
spl set id: b210f5da-d4d9-49dd-8947-220040ab32e1

Reported adverse events (FAERS/openFDA)#

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