FDA.reportPublic FDA data

Jack Black Clearing Spot Treatment

Manufacturer
Jack Black LLC
Effective date
2025-01-08
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
legacy-cache
Hydrated at
2026-08-01 20:43:08

Label at a glance#

ProductJack Black Clearing Spot Treatment
Active ingredientSULFUR
Label structure6 sections

Indications and uses

For the treatment of acne Dries and clears acne blemishes and blackheads and allows skin to heal.

Dosage and administration

Clean the skin thoroughtly before applying this product cover the entire ara with a thin layer one to three times daily Because excess 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

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Sulfur 10%

Purpose

OTC - PURPOSE SECTION

Acne Treatment

Uses

INDICATIONS & USAGE SECTION

  • For the treatment of acne
  • Dries and clears acne blemishes and blackheads and allows skin to heal.

Warnings

WARNINGS SECTION

  For external use only

When using this product

OTC - WHEN USING SECTION

  • apply only to areas with acne
  • 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 medication at a time.
  • avoid product contact with silver jewelry.
Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Do Not Use

OTC - DO NOT USE SECTION

  • On broken skin
  • on large areas of the skin

Directions

DOSAGE & ADMINISTRATION SECTION

  • Clean the skin thoroughtly before applying this product
  • cover the entire ara with a thin layer one to three times daily
  • Because excess 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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, C12-15 Alkyl Benzoate, Glycerin, Caprylic/Capric Triglyceride, Acacia Senegal Gum, Magnesium Aluminum Silicate, Glyceryl Stearate,
PEG-100 Stearate, Pentylene Glycol, Phenoxyethanol, Butylene Glycol, Decylene Glycol, Zinc PCA, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Xanthan Gum, Sodium PCA, Isohexadecane, Ganoderma Lucidum Extract, Sodium Hydroxide, Bisabolol, Ethylhexylglycerin, Polysorbate 80, Lysine, Propanediol, Aloe Barbadensis Leaf Juice, Tetrasodium Glutamate Diacetate, Curcuma Longa (Turmeric) Root Extract, Camellia Sinensis Leaf Extract, 10-Hydroxydecanoic Acid, Sebacic Acid, Magnesium Chloride, Potassium Chloride,
Sodium Chloride, 1,10-Decanediol, Zinc Chloride

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SptTrtmntUCSptTrtmntUC

Products#

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

DailyMed product names page 1 of 1 · 37 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66738-43666738-436-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 36 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
GLYCERINPDC6A3C0OXIACT
PROPANEDIOL5965N8W85TIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
CURCUMA LONGA WHOLEW5488JUO8UIACT
CAMELLIA SINENSIS FLOWER9I2BJY2J17IACT
ALOEV5VD430YW9IACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
ACACIA SENEGAL FLOWER72P931MTC2IACT
MAGNESIUM ALUMINUM SILICATE6M3P64V0NCIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
PEG-100 STEARATEYD01N1999RIACT
PENTYLENE GLYCOL50C1307PZGIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
PHENOXYETHANOLHIE492ZZ3TIACT
DECYLENE GLYCOLS57M60MI88IACT
ZINC PIDOLATEC32PQ86DH4IACT
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW)1DXE3F3OZXIACT
XANTHAN GUMTTV12P4NEEIACT
SODIUM PYRROLIDONE CARBOXYLATE469OTG57A2IACT
ISOHEXADECANE918X1OUF1EIACT
GANODERMA LUCIDUM WHOLEJ5P04QW0CFIACT
SODIUM HYDROXIDE55X04QC32IIACT
LEVOMENOL24WE03BX2TIACT
POLYSORBATE 806OZP39ZG8HIACT
LYSINEK3Z4F929H6IACT
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
10-HYDROXYDECANOIC ACIDNP03XO416BIACT
SEBACIC ACID97AN39ICTCIACT
MAGNESIUM CHLORIDE02F3473H9OIACT
POTASSIUM CHLORIDE660YQ98I10IACT
SODIUM CHLORIDE451W47IQ8XIACT
1,10-DECANEDIOL5I577UDK52IACT
ZINC CHLORIDE86Q357L16BIACT
SULFUR70FD1KFU70ACTIB

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
2b3874e6-d960-01fe-e063-6394a90ab98b10b6eccd-ecb0-4505-9e59-78f0ba03abcd2025-01-08WarningsExact identifier
spl id: 2b3874e6-d960-01fe-e063-6394a90ab98b
spl set id: 10b6eccd-ecb0-4505-9e59-78f0ba03abcd

Reported adverse events (FAERS/openFDA)#

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