SULFUR (clarifying detox- acne treatment mask cream

Sulfur by

Drug Labeling and Warnings

Sulfur by is a Otc medication manufactured, distributed, or labeled by Vege Labs LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Sulfur 3.0%

Purpose

Acne Treatment

Uses

For the management of acne

Warnings

For external use only

Do not use on

Broken skin, Large areas of the skin

When using this product

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. Apply only to areas with acne

Keep out of reach of children

If product is swallowed, get medical help or contact a poison control center right away

Directions

Clean the skin thoroughly before applying this product. Cover the entire affected area with a thin layer. Leave on for 10-15 minutes, rinse thoroughly, and pat dry. Because excessive drying of the skin may occur, start with one application weekly then gradually increase to two or three times weekly if needed or as directed by a doctor. If bothersome dryness or peeing occurs, reduce application to once a week or every other week.

Inactive Ingredients

Water, Illite, Glycerin, Propanediol, Magnesium Aluminum Silicate, Caolin, Ethyl Linoleate, Glyceryl Stearate, Cetearyl Alcohol, Ceteareth-20, PEG-100 Stearate, Microcrystalline Wax, Potassium Azeloyl Diglycinate, Morinda Citrifolia Extract, Citrullus Lanatus (Watermelon) Fruit Extract, Menthol, Camellia Sinensis Leaf Extract, Pyrus Malus (Apple) Fruit Extract, Lens Esculenta (Lentil) Fruit Extract, Sodium Lactate, Sodium PCA, Citrus Aurantium Bernamia (Bergamot) Peel Oil, Polyisobutene, Caprylyl/Capryl Glucoside, Sorbitan Oleat, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Caprylyl Glycol, Ethylhexylglycerin, Potassium Chloride, Citric Acid, Disodium EDTA, Xanthan Gum, Chlorphenesin, Potassium Sorbate, Sodium Benzoate, Phenoxyethanol, Chromium Oxide Greens

Lancer Acne Mask 0.25 fl oz

INGREDIENTS AND APPEARANCE

SULFUR 
clarifying detox (acne treatment) mask cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67923-106
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	3 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID (UNII: 2968PHW8QP)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
SODIUM BENZOATE (UNII: OJ245FE5EU)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ILLITE (UNII: D7BC5B0F46)
POTASSIUM AZELOYL DIGLYCINATE (UNII: N02RVN6NYP)
XANTHAN GUM (UNII: TTV12P4NEE)
MORINDA CITRIFOLIA FRUIT (UNII: 7829X3G2X5)
CITRULLUS LANATUS WHOLE (UNII: 3J5I6254YO)
MENTHOL (UNII: L7T10EIP3A)
SODIUM PCA (UNII: 469OTG57A2)
CITRUS AURANTIUM BERGAMIA (BERGAMOT) PEEL OIL (UNII: 39W1PKE3JI)
LENTIL (UNII: 6O38V6B52O)
CAPRYLYL/CAPRYL GLUCOSIDE (UNII: E00JL9G9K0)
SORBITAN OLEATE (UNII: 06XEA2VD56)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
KAOLIN (UNII: 24H4NWX5CO)
PYRUS MALUS (APPLE) FRUIT (UNII: B423VGH5S9)
SODIUM LACTATE (UNII: TU7HW0W0QT)
ETHYL LINOLEATE (UNII: MJ2YTT4J8M)
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
CAMELLIA SINENSIS LEAF (UNII: W2ZU1RY8B0)
HYDROGENATED POLYISOBUTENE (450 MW) (UNII: 7YR4ZFS62E)
PROPANEDIOL (UNII: 5965N8W85T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
CETEARETH-20 (UNII: YRC528SWUY)
CHROMIUM OXIDE GREENS (UNII: X5Z09SU859)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
PEG-100 STEARATE (UNII: YD01N1999R)
CALCIUM DISODIUM EDTA (UNII: 8U5D034955)
CHLORPHENESIN (UNII: I670DAL4SZ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67923-106-05	1 in 1 CARTON	01/25/2020
1		7.5 mg 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	01/25/2020

Labeler - Vege Labs LLC (117878620)

Establishment
Name	Address	ID/FEI	Business Operations
Vege Labs LLC		117878620	manufacture(67923-106)