CLARIFYING SPOT WITH SULFUR PLUS GREEN CLAY  ACNE MEDICATION- sulfur solution 
Lancer Skincare 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.

----------

Clarifying Spot with Sulfur plus Green Clay
Acne Medication

Drug Facts

Active Ingredient

Sulfur 10.0%

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.

Flammable, keep away from fire or flame.

Directions

Inactive Ingredients

Alcohol Denat., Water, Azelaic Acid, PVP, Camellia Sinensis Leaf Extract, Salicylic Acid, Papain, Bromelain, Maltodextrin, Glycerin, Magnesium Aluminum Silicate, Disodium Carboxyethyl Siliconate, Illite, Montmorillonite, Kaolin, Calcite, Sodium Hydroxide, Chromium Oxide Greens, Titanium Dioxide

Questions?

1800-899-0744 M-F 9-5PST

Dist. by
LANCER SKINCARE LLC
440 N. Rodeo Dr., 3F
Beverly Hills, CA 90210

PRINCIPAL DISPLAY PANEL - 9 mL Tube Carton

LANCER®

RESEARCHED
AND DEVELOPED
AT
LANCERX
dermatology
BEVERLY HILLS

• UTMOST LUXURY
• LANCER SKINCARE
• FIRST-CLASS DERMATOLOGY
• TRUE EFFICACY

CLARIFYING SPOT
SOLUTION
with 10% Sulfur + Green Clay

0.3 FL.OZ. | 9 mL

PRINCIPAL DISPLAY PANEL - 9 mL Tube Carton
CLARIFYING SPOT WITH SULFUR PLUS GREEN CLAY   ACNE MEDICATION
sulfur solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72704-129
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Sulfur (UNII: 70FD1KFU70) (Sulfur - UNII:70FD1KFU70) Sulfur10 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Alcohol (UNII: 3K9958V90M)  
Water (UNII: 059QF0KO0R)  
Azelaic Acid (UNII: F2VW3D43YT)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
Green Tea Leaf (UNII: W2ZU1RY8B0)  
Salicylic Acid (UNII: O414PZ4LPZ)  
Papain (UNII: A236A06Y32)  
Bromelains (UNII: U182GP2CF3)  
Maltodextrin (UNII: 7CVR7L4A2D)  
Glycerin (UNII: PDC6A3C0OX)  
Magnesium Aluminum Silicate (UNII: 6M3P64V0NC)  
Disodium Carboxyethyl Siliconate (UNII: 4U4C79679G)  
Ledikite (UNII: D7BC5B0F46)  
Montmorillonite (UNII: A585MN1H2L)  
Kaolin (UNII: 24H4NWX5CO)  
Calcium Carbonate (UNII: H0G9379FGK)  
Sodium Hydroxide (UNII: 55X04QC32I)  
Chromic Oxide (UNII: X5Z09SU859)  
Titanium Dioxide (UNII: 15FIX9V2JP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72704-129-011 in 1 CARTON10/15/2021
19 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart333D10/15/2021
Labeler - Lancer Skincare LLC. (079089155)
Establishment
NameAddressID/FEIBusiness Operations
Vege-Labs117878620MANUFACTURE(72704-129)

Revised: 1/2023
Document Id: 1decc807-6919-498c-89d1-4c048c3bf3e0
Set id: 4948e2d1-7dc9-484c-bc27-eba511323179
Version: 2
Effective Time: 20230119
 
Lancer Skincare LLC.