EARTHS CARE ACNE SPOT TREATMENT- sulfur cream 
DLC Laboratories, Inc.

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.

----------

Earths Care Acne Spot Treatment

Drug Facts

Active ingredient

Sulfur 10%

Purpose

Acne medication

Uses

for the treatment of acne

Warnings

For external use only

When using this product

  • do not get into eyes
  • 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

Do not use on

  • broken skin
  • large areas of the skin

Stop use and ask a doctor if

  • excessive skin irritation develops or increases

Keep out of reach of children.

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

Directions

Inactive ingredients

Avena sativa (oat) kernel colloidal oatmeal, bentonite, Butyrospermum parkii (shea) butter, cetearyl glucoside, citric acid, glycerin, glyceryl stearate, Helianthus annuus (sunflower) seed oil, hydrogenated castor oil, phenoxyethanol, potassium sorbate, purified water, sodium stearoyl glutamate, xanthan gum

Questions

1-888-602-6380

Distributed by:
Earth's Care Natural Products, Inc.
Long Beach, California 90805 USA

PRINCIPAL DISPLAY PANEL - 27 g Tube Box

Allergy Tested

EARTH'S CARE ®

* PARABEN * FREE

Acne Spot Treatment

Maximum Strength

Sulfur 10%

Clears and Helps Prevent
Stubborn Blemishes

with Natural Bentonite
and Colloidal Oatmeal

Non-Comedogenic

1% FOR THE PLANET SM MEMBER

0.97 OZ. (27 g) Acne-Spot-treatment

EARTHS CARE ACNE SPOT TREATMENT 
sulfur cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24286-1557
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR10 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
OATMEAL (UNII: 8PI54V663Y)  
BENTONITE (UNII: A3N5ZCN45C)  
SHEA BUTTER (UNII: K49155WL9Y)  
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
SUNFLOWER OIL (UNII: 3W1JG795YI)  
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
WATER (UNII: 059QF0KO0R)  
SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24286-1557-11 in 1 BOX01/18/2013
127 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:24286-1557-22.8 g in 1 POUCH; Type 0: Not a Combination Product01/18/2013
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D01/18/2013
Labeler - DLC Laboratories, Inc. (093351930)
Establishment
NameAddressID/FEIBusiness Operations
DLC Laboratories, Inc.093351930manufacture(24286-1557)

Revised: 1/2022
Document Id: d554be20-c277-1b60-e053-2a95a90a950e
Set id: 85dab75e-5436-4e31-9ce2-c1995fde1dd9
Version: 4
Effective Time: 20220111
 
DLC Laboratories, Inc.