SULPHO-LAC MEDICATED

Dosage form: soap
Ingredients: SULFUR 5.0g in 100g
Labeler: Bradford Soap Works, Inc.
NDC Code: 11118-1008

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.

ACTIVE INGREDIENTSULFUR  5 %

PURPOSE

ACNE TREATMENT SOAP

INDICATIONSFOR USE IN THE MANAGEMENT OF ACNE

  • CLEARS UP BLACKHEADS AND ACNE PIMPLES AND ALLOWS SKIN TO HEAL
  • HELPS PREVENT NEW BLACKHEADS AND ACNE PIMPLES FROM FORMING

WARNINGS FOR EXTERNAL USE ONLY

WHEN USING THIS PRODUCT
  • DO NOT GET INTO EYES
  • IF EXCESSIVE SKIN IRRITATION DEVELOPS OR INCREASES, DISCONTINUE USE AND CONSULT A PHYSICIAN
  • USING OTHER TOPICAL ACNE MEDICATIONS AT THE SAME TIME OR IMMEDIATELY FOLLOWING USE OF THIS PRODUCT MAY INCREASE DRYNESS OR IRRITATION OF THE SKIN.  IF THIS OCCURS ONLY ONE MEDICATION SHOULD BE USED UNLESS OTHERWISE DIRECTED BY A PHYSICAN

DIRECTIONS
  • GENTLY WASH AFFECTED AREA WITH SULPHO-LAC MEDICATED SOAP.  ALLOW LATHER TO REMAIN ON SKIN FOR THREE TO FIVE MINUTES
  • RINSE THOROUGHLY WITH WARM WATER AND GENTLY PAT DRY WITH  CLEAN TOWEL
  • MAY BE USED FROM ONE TO THREE TIMES A DAY
  • BECAUSE EXCESSIVE DRYNESS OF THE SKIN MAY OCCUR, START WITH ONE APPLICATION A DAY, THEN GRADUALLY INCREASE TO TWO OR THREE TIMES DAILY, IF NEEDED, OR AS DIRECTED BY A PHYSICIAN

OTHER INFORMATION

STORE AT ROOM TEMPERATURE  150 - 300 C (590 - 860 F).

INACTIVE INGREDIENTS

SODIUM TALLOWATE, SODIUM COCOATE, PURIFIED WATER, PENTASODIUM PENTETATE, TETRASODIUM ETIDRONATE, SODIUM PALM KERNELATE

PACKAGE IMAGE




SULPHO-LAC MEDICATED 
sulfur soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11118-1008
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SULFUR (SULFUR) SULFUR5.0 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
COCONUT OIL 
WATER 
GLYCERIN 
PENTASODIUM PENTETATE 
ETIDRONATE TETRASODIUM 
Packaging
#Item CodePackage Description
1NDC:11118-1008-885 g in 1 BOX
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33302/20/2007
Labeler - Bradford Soap Works, Inc. (001201045)
Registrant - Bradford Soap Works, Inc. (001201045)
Establishment
NameAddressID/FEIOperations
Bradford Soap Works, Inc.001201045manufacture, label
Establishment
NameAddressID/FEIOperations
The Original Bradford Soap Works, Inc362189503manufacture, label
Establishment
NameAddressID/FEIOperations
Jean Charles Mexicali SA de C.V.824250179manufacture, label

Revised: 01/2010
 
Bradford Soap Works, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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