TINEACIDE SOLUTION

Dosage form: liquid
Ingredients: TOLNAFTATE 1mL in 100mL
Labeler: Blaine Labs Inc.
NDC Code: 63347-511

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 INGREDIENTS

TOLNAFTATE 1%

INACTIVE INGREDIENTS

SAFFLOWER OIL, MINERAL OIL, JOJOBA OIL, BHT, BHA, COLLOIDAL SILVER, TOCOPHERYL ACETATE, METHYL PARABEN, PROPYL PARABEN

PURPOSE SECTION

ANTIFUNGAL TREATMENT

INDICATIONS

INDICATIONS: TINEACIDE SOLUTION CURES MOST DERMATOPHYTOSIS (ATHLETE'S FOOT), TINEA CRURIS (JOCK ITCH) AND TINEA CORPORIS (RINGWORM).

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN. IN CASE OF ACCIDENTAL INGESTION CONTACT A POISON CONTROL CENTER IMMEDIATELY.

DOSAGE AND ADMINISTRATION

WASH THE AFFECTED AREA AND DRY THOROUGHLY. APPLY A THIN LAYER OVER AFFECTED AREA TWICE DAILY (MORNING AND NIGHT) OR AS DIRECTED BY A PHYSICIAN. SUPERVISE CHILDREN IN THE USE OF THE PRODUCT.

FOR ATHLETE'S FOOT: PAY SPECIAL ATTENTION TO SPACES BETWEEN THE TOES; WEAR WELL-FITTING, VENTILATED SHOES, AND CHANGE SOCKS AND SHOES AT LEAST ONCE DAILY. FOR ATHLETE'S FOOT AND RING WORM: USE DAILY FOR 4 WEEKS. FOR JOCK ITCH: USE DAILY FOR 2 WEEKS. IF CONDITION PERSISTS LONGER, CONSULT A PHYSICIAN.

WARNINGS

WARNINGS: DO NOT USE ON CHILDREN UNDER 2 YEARS OF AGE UNLESS DIRECTED BY A PHYSICIAN. FOR EXTERNAL USE ONLY. AVOID CONTACT WITH EYES. STOP USE AND CONSULT A PHYSICIAN IF IRRITATION OCCURS OR IF THERE IS NO IMPROVEMENT WITHIN 4 WEEKS (FOR ATHLETE'S FOOT OR RINGWORM) OR WITHIN 2 WEEKS (FOR JOCK ITCH).

TINEACIDE SOLUTION LABEL

TINEACIDE SOLUTION PHYSICIAN FORMULA ANTIFUNGAL TREATMENT

NET CONTENTS 1/2 FL. OZ. (15 ML)

BLAINE LABS, INC. SANTA FE SPRINGS, CA 90670 800-307-8818 INFO@BLAINELABS.COM

27000-P-L REV. 20110602

TINEACIDE SOLUTION 
tolnaftate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63347-511
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TOLNAFTATE (TOLNAFTATE) TOLNAFTATE1 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
SAFFLOWER OIL 
MINERAL OIL 
JOJOBA OIL 
BUTYLATED HYDROXYTOLUENE 
BUTYLATED HYDROXYANISOLE 
SILVER 
.ALPHA.-TOCOPHEROL ACETATE, D- 
METHYLPARABEN 
PROPYLPARABEN 
Packaging
#Item CodePackage Description
1NDC:63347-511-0115 mL in 1 BOTTLE, WITH APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C01/01/1995
Labeler - Blaine Labs Inc. (017314571)
Registrant - Blaine Labs Inc. (017314571)
Establishment
NameAddressID/FEIOperations
Blaine Labs Inc.017314571manufacture

Revised: 06/2011
 
Blaine Labs 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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