DR CANUSO FUNGAL NAIL ERASER- tolnaftate oil oil

Dr CANUSO fungal nail eraser by

Drug Labeling and Warnings

Dr CANUSO fungal nail eraser by is a Otc medication manufactured, distributed, or labeled by Renu Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Tolnaftate 1%

PURPOSE

Purpose

Antifungal

Uses

• Helps cure most fungal nail and skin infections including Fungus (Tinea Pedis)
• Effectively relieves cracking, scaling and soreness accompanying the above conditon

WARNINGS

Warnings

For external use only

• Do not use on children under 2 years of age unless directed by a doctor
• Avoid contact with eyes, ears or mouth
• Stop use and ask a physician if rash or irritation occurs

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

PREGNANCY OR BREAST FEEDING

If pregnant or breastfeeding ask a health Professional before use

Directions

• Trim nails and file the surface of nails using an emory board
• Apply a thin layer of the product over affected areas twice daily (morning and night) especially around free edges of nails (under tips) and cuticles and the space around the toenails.
• Allow solution to soak into nail or skin
• Application to adjacent nails is recommended to prevent the spread of infection
• Keep affected areas clean and dry throughout the day
• Supervise children in the use of this product

INACTIVE INGREDIENT

Inactive Ingredients

Cinnamomum Zeylanicum (Cinnamon Leaf) Oil, Ethoxydiglycol, Ethyl Macadamiate, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Olea Europaea (Olive Oil), Trimethylpentanediol/Adipic Acid Copolymer.

QUESTIONS

Questions or Comments?

Visit www.DrCanuso.com

DOSAGE & ADMINISTRATION

Uses

• Helps cure most fungal nail and skin infections including Athlete's Foot (Tinea Pedis)
• Effectively relieves cracking, scaling and soreness accompanying the above condition

LABEL FOR BOTTLED PRODUCT

Product BOX

INGREDIENTS AND APPEARANCE

DR CANUSO FUNGAL NAIL ERASER 
tolnaftate oil oil

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76348-410
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV)	TOLNAFTATE	0.3 g  in 28 g

Inactive Ingredients
Ingredient Name	Strength
ETHYL MACADAMIATE (UNII: ANA2NCS6V1)
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
CINNAMON LEAF OIL (UNII: S92U8SQ71V)
TEA TREE OIL (UNII: VIF565UC2G)
TRIMETHYLPENTANEDIOL/ADIPIC ACID/GLYCERIN CROSSPOLYMER (25000 MPA.S) (UNII: 587WKM3S9Q)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
OLIVE OIL (UNII: 6UYK2W1W1E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76348-410-02	1 in 1 BOX	08/11/2015
1		14 g in 1 BOTTLE, GLASS; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333C	08/11/2015

Labeler - Renu Laboratories, Inc. (945739449)

Establishment
Name	Address	ID/FEI	Business Operations
Renu Laboratories, Inc.		945739449	manufacture(76348-410)