DHC Acne Spot Therapy

Manufacturer
DHC USA Incorporated | ABBE Laboratories, Inc.
Effective date
2026-01-24
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:34:38

Label at a glance#

ProductDHC Acne Spot Therapy
Active ingredientSulfur
Label structure10 sections

Indications and uses

For the management of acne. Helps clear up acne blemishes.

Dosage and administration

Cleanse skin thoroughly and tone before applying. Cover the affected area with a thin layer one to three times daily. Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two to 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.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Sulfur 3%

Purpose

OTC - PURPOSE SECTION

Acne treatment

Uses

INDICATIONS & USAGE SECTION

For the management of acne. Helps clear up acne blemishes.

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

  • When using this product skin irritation and dryness is more likely to occur if used with 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 excessive skin irritation develops or increases, discontinue use and consult a doctor.

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.

OTC - DO NOT USE SECTION

Do not use on

  • Broken skin
  • Large areas of the skin

When using this product

OTC - WHEN USING SECTION

  • Apply only to areas with acne

Directions

DOSAGE & ADMINISTRATION SECTION

Cleanse skin thoroughly and tone before applying. Cover the affected area with a thin layer one to three times daily. Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two to 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

water, butylene glycol, isononyl isononanoate, cetearyl alcohol, sorbitan stearate, ceteareth-20, phenoxyethanol, sucrose cocoate, xanthan gum, sodium citrate, citric acid, allantoin, disodium EDTA, magnesium ascorbyl phosphate, tocopherol, sodium hydroxide, brassica campestris (rapeseed) seed oil, glycyrrhiza glabra (licorice) root extract, camellia sinensis leaf extract, royal jelly extract, scutellaria baicalensis root extract, houttuynia cordata extract, perilla ocymoides leaf extract, aloe barbadensis leaf extract

Questions or Comments?

OTC - QUESTIONS SECTION

800-DHC-CARE (342-2273)
dhccare.com

SPL UNCLASSIFIED SECTION

Distributed by DHC USA Inc.
Mechanicsburg, PA 17050

PRINCIPAL DISPLAY PANEL - 15 g Tube Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DHC

Acne
Spot Therapy

Acne Treatment

.52 oz. (15 g) Net wt.

PRINCIPAL DISPLAY PANEL - 15 g Tube Box
PRINCIPAL DISPLAY PANEL - 15 g Tube Box

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
199632sulfur 3 % Topical CreamPSN4
199632sulfur 30 MG/ML Topical CreamSCD4
199632sulfur 3 % Topical CreamSY4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63433-389-002022-03-15C16284748780-19d75b9d1-1f0e-f424-e053-dadaa90a57ceDHC Acne Spot Therapy
63433-389-002020-01-31C16284748780-19d75b9d1-1f0e-f424-e053-dadaa90a57ceDHC Acne Spot Therapy

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63433-389-00DHC Acne Spot Therapy15 g in 1 TUBECREAM154

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63433-38963433-389-00

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
DHC Acne Spot TherapySULFURDHC USA Incorporated84d49048-95cf-4f14-9698-c746237fec9d2026-01-24WarningsExact identifier
ndc (package): 63433-389-00
ndc (product): 63433-389
ndc11 (package): 63433038900
spl id: 4ae85fb3-936c-45b4-95d9-b3206952cd94
spl set id: 84d49048-95cf-4f14-9698-c746237fec9d

Reported adverse events (FAERS/openFDA)#

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