DEEP ACNE- sulfur gel 
Dermalogica, LLC.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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DEEP ACNE LIQUID PATCH

Drug Facts

Active Ingredients

Sulfur...5.00%

Purpose

Acne Treatment

Use

Warnings

For external use only

Do not use

  • On broken skin or large areas of the skin.

When using this product

  • Apply only to areas with acne.
  • Skin irritation and dryness are 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.

Keep out of reach of children.

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

Directions

Inactive ingredients

Water/Aqua/Eau, Niacinamide, Propanediol, Glycerin, Acacia Senegal Gum, Polyacrylate Crosspolymer-6, Hydroxyacetophenone, Lactic Acid, Pelargonium Graveolens Flower Oil, Lavandula Hybrida Oil, Lavandula Angustifolia (Lavender) Oil, Citrus Limon (Lemon) Peel Oil, Salvia Sclarea (Clary) Oil, Aloe Barbadensis Leaf Extract, Citrus Aurantium Dulcis (Orange) Peel Oil, Punica Granatum Pericarp Extract, Rosmarinus Officinalis (Rosemary) Leaf Oil, Myristyl Myristate, Beta-Glucan, Biosaccharide Gum-1, Glyceryl Stearate, Maltodextrin, Caprylyl Glycol, Polylysine, Cetearyl Alcohol, 1,2-Hexanediol, Sodium Acrylates Crosspolymer-2, Ceteareth-12, Titanium Dioxide, Tetrasodium Glutamate Diacetate, Potassium Cetyl Phosphate, Sodium Hydroxide, Dimethyl Isosorbide, Thymol, Terpineol, Algin, Camphor, O-Cymen-5-Ol, Sodium Benzoate, Limonene, Linalool, Citronellol, Geraniol.

Questions or comments

Call toll free 1-800-831-5150 in the US

PRINCIPAL DISPLAY PANEL - 15 mL Tube Carton

deep acne
liquid patch

with 5% sulfur +
camphor

invisible
acne
treatment

dermalogica

Active Clearing

0.5 US FL OZ / 15 mL e

PRINCIPAL DISPLAY PANEL - 15 mL Tube Carton
DEEP ACNE 
sulfur gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68479-240
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Sulfur (UNII: 70FD1KFU70) (Sulfur - UNII:70FD1KFU70) Sulfur5 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Niacinamide (UNII: 25X51I8RD4)  
Propanediol (UNII: 5965N8W85T)  
Glycerin (UNII: PDC6A3C0OX)  
ACACIA (UNII: 5C5403N26O)  
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)  
Myristyl Myristate (UNII: 4042ZC00DY)  
Maltodextrin (UNII: 7CVR7L4A2D)  
Dimethyl Isosorbide (UNII: SA6A6V432S)  
Sodium Acrylates Crosspolymer-2 (UNII: D3HPR4WW6F)  
Hydroxyacetophenone (UNII: G1L3HT4CMH)  
Ceteareth-12 (UNII: 7V4MR24V5P)  
LACTIC ACID, DL- (UNII: 3B8D35Y7S4)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
o-Cymen-5-ol (UNII: H41B6Q1I9L)  
Titanium Dioxide (UNII: 15FIX9V2JP)  
Tetrasodium Glutamate Diacetate (UNII: 5EHL50I4MY)  
ORANGE OIL, COLD PRESSED (UNII: AKN3KSD11B)  
Pelargonium Graveolens Flower Oil (UNII: 3K0J1S7QGC)  
SODIUM ALGINATE (UNII: C269C4G2ZQ)  
Terpineol (UNII: R53Q4ZWC99)  
Thymol (UNII: 3J50XA376E)  
POMEGRANATE FRUIT RIND (UNII: RS999V57DU)  
LAVENDER OIL (UNII: ZBP1YXW0H8)  
LAVANDIN OIL (UNII: 9RES347CKG)  
Sodium Benzoate (UNII: OJ245FE5EU)  
1,2-Hexanediol (UNII: TR046Y3K1G)  
Biosaccharide Gum-1 (UNII: BB4PU4V09H)  
Caprylyl Glycol (UNII: 00YIU5438U)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
Potassium Cetyl Phosphate (UNII: 03KCY6P7UT)  
CAMPHOR (NATURAL) (UNII: N20HL7Q941)  
LEMON OIL, DISTILLED (UNII: ET5GD00TRP)  
ROSEMARY OIL (UNII: 8LGU7VM393)  
CLARY SAGE OIL (UNII: 87L0D4U3M0)  
Sodium Hydroxide (UNII: 55X04QC32I)  
LIMONENE, (+)- (UNII: GFD7C86Q1W)  
LINALOOL, (+/-)- (UNII: D81QY6I88E)  
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
Geraniol (UNII: L837108USY)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68479-240-021 in 1 CARTON12/01/2022
115 mL in 1 TUBE; Type 0: Not a Combination Product
2NDC:68479-240-002 mL in 1 POUCH; Type 0: Not a Combination Product12/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D12/01/2022
Labeler - Dermalogica, LLC. (177698560)
Establishment
NameAddressID/FEIBusiness Operations
McKenna090631412MANUFACTURE(68479-240)

Revised: 11/2022
Document Id: 6df854ae-1949-4b52-9208-b82fc73d8b7d
Set id: d4e9d230-2ee4-4cc7-a7c9-a7dde50b6f40
Version: 1
Effective Time: 20221118
 
Dermalogica, LLC.