Jack Black Acne Remedy Clearing Spot Treatment

Jack Black Clearing Spot Treatment by

Drug Labeling and Warnings

Jack Black Clearing Spot Treatment by is a Otc medication manufactured, distributed, or labeled by Jack Black LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

JACK BLACK CLEARING SPOT TREATMENT- sulfur gel 
Jack Black LLC

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Jack Black Acne Remedy Clearing Spot Treatment

Active Ingredients

Sulfur 10%

Purpose

Acne Treatment

Uses

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

Warnings

  For external use only

When using this product

• 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.

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

Do Not Use

• On broken skin
• on large areas of the skin

Directions

• 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

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

JACK BLACK CLEARING SPOT TREATMENT 
sulfur gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66738-436
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	0.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
GLYCERIN (UNII: PDC6A3C0OX)
PROPANEDIOL (UNII: 5965N8W85T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CURCUMA LONGA WHOLE (UNII: W5488JUO8U)
CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17)
ALOE (UNII: V5VD430YW9)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
ACACIA SENEGAL FLOWER (UNII: 72P931MTC2)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
PEG-100 STEARATE (UNII: YD01N1999R)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
DECYLENE GLYCOL (UNII: S57M60MI88)
ZINC PIDOLATE (UNII: C32PQ86DH4)
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
XANTHAN GUM (UNII: TTV12P4NEE)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
ISOHEXADECANE (UNII: 918X1OUF1E)
GANODERMA LUCIDUM WHOLE (UNII: J5P04QW0CF)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
LEVOMENOL (UNII: 24WE03BX2T)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
LYSINE (UNII: K3Z4F929H6)
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
10-HYDROXYDECANOIC ACID (UNII: NP03XO416B)
SEBACIC ACID (UNII: 97AN39ICTC)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
1,10-DECANEDIOL (UNII: 5I577UDK52)
ZINC CHLORIDE (UNII: 86Q357L16B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66738-436-01	1 in 1 CARTON	02/12/2021	02/22/2025
1		15 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	02/12/2021	02/22/2025

Labeler - Jack Black LLC (847024036)

Revised: 1/2025

Document Id: 2b3874e6-d960-01fe-e063-6394a90ab98b

34390-5

Set id: 10b6eccd-ecb0-4505-9e59-78f0ba03abcd

Version: 10

Effective Time: 20250108