OTC Medication Information: CAREALL Tolnaftate

CAREALL TOLNAFTATE- tolnaftate cream
New World Imports, Inc

Tolnaftate 1%

Antifungal

Keep out of reach of children. If Swallowed, get medical help or contact a Poison Control center right away.

  • Proven clinically effective in the treatment of athlete’s foot (tinea pedis), jock itch (tinea cruris), ringworm (tinea corporis)
  • For effective relief of itching, burning and cracking

For external use only

When using this product avoid contact with the eyes

Stop use and ask a doctor if

  • irritation occurs
  • there is no improvement within 4 weeks (for athlete’s foot or ring worm) or 2 weeks (for jock itch).

Do not use on children under 2 years of age unless directed by a doctor

  • Wash affected area and dry thoroughly
  • Apply a thin layer over affected area twice daily (morning and night) or as directed by a doctor
  • Supervise children in the use of this product
  • for athlete’s foot, pay special attention to spaces between the toes, wear well-fitting, ventilated shows and change shoes and socks at least once daily
  • For athlete’s foot and ringworm use daily for 4 weeks, for jock itch use daily for 2 weeks.
  • If condition persists longer consult a doctor
  • This product is not effective on scalp or nails

Ceteth 20, Cetyl Alcohol, Methylparaben, Mineral Oil, Propylene Glycol, Propylparaben, Sorbitan Monostearate, Steryl Alcohol, Purified Water

Tolnaftate label
(click image for full-size original)

CAREALL TOLNAFTATE
tolnaftate cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:51824-001
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Tolnaftate (Tolnaftate) Tolnaftate 10 mg in 1 g
Inactive Ingredients
Ingredient Name Strength
Propylene Glycol
Mineral Oil
Stearyl Alcohol
Cetyl Alcohol
Sorbitan Monostearate
Ceteth-20
Water
Methylparaben
Propylparaben
Product Characteristics
Color white Score
Shape Size
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:51824-001-05 14 g in 1 TUBE None
2 NDC:51824-001-01 28 g in 1 TUBE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC Monograph Drug M005 06/01/2012
Labeler — New World Imports, Inc (075372276)

Revised: 01/2024 New World Imports, Inc

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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