DR. CANUSO FOOT REPAIR SERUM- tolnaftate serum lotion

Dr. Canuso foot repair serum by

Drug Labeling and Warnings

Dr. Canuso foot repair serum by is a Otc medication manufactured, distributed, or labeled by Renu Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Tolnaftate 1%

PURPOSE

Antifungal

WARNINGS

When using this product

• Do not use on children under 2 years of age unless directed by a doctor
• Avoid contact with eyes
• If irritation occurs, discontinue use and consult a doctor
• If swallowed, get medical help or consult a poison control center immediately

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

STORAGE AND HANDLING

Other Information

Store at room temperature (59-86º F)

INACTIVE INGREDIENT

Inactive Ingredients

Acetylated Lanolin Alcohol, Acryloyldimethyl Taurate Copolymer, Benzoic Acid, Cetyl Acetate, Cyclopentasiloxane, Dehydroacetic Acid, Deionized Water, Dimethiconol, Ethoxydiglycol, Glycerin, Menthol, Menthyl Lactate, Olea Europaea (Olive Oil), PEG-12 Dimethicone, Phenoxyethanol, Phenyl Trimethicone, Polysorbate 60, Polysorbate 80, Propylene Glycol, Squalane, Talc.

QUESTIONS

Questions or Comments?
Visit www.DrCanuso.com

INDICATIONS & USAGE

Directions

• Apply two pumps of serum onto each foot morning and night, paying special attention to rough cracked skin.
• For maintenance of smooth skin, massage two pumps of serum into each foot once daily.
• Supervise children in the use of this product.

DOSAGE & ADMINISTRATION

Directions

• Apply two pumps of serum onto each fot morning and night, paying special attention to rough cracked skin.

BOX ART_76348-407-02

BOTTLE LABEL - Bottle resides in BOX

INGREDIENTS AND APPEARANCE

DR. CANUSO FOOT REPAIR SERUM 
tolnaftate serum lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76348-409
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
OLIVE OIL (UNII: 6UYK2W1W1E)
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
MENTHOL (UNII: L7T10EIP3A)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
TALC (UNII: 7SEV7J4R1U)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)
GLYCERIN (UNII: PDC6A3C0OX)
CETYL ACETATE (UNII: 4Q43814HXS)
ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P)
WATER (UNII: 059QF0KO0R)
MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)
DIMETHICONE (UNII: 92RU3N3Y1O)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
2-HYDROXYETHYL ACRYLATE (UNII: 25GT92NY0C)
SODIUM ACRYLOYLDIMETHYLTAURATE (UNII: 2T9Q6EKI0G)
SQUALANE (UNII: GW89575KF9)
POLYSORBATE 60 (UNII: CAL22UVI4M)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZOIC ACID (UNII: 8SKN0B0MIM)

Product Characteristics
Color	white (Serum)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76348-409-02	1 in 1 BOX	08/20/2015
1		28 g in 1 BOTTLE, PUMP; 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	08/20/2015

Labeler - Renu Laboratories, Inc. (945739449)

Establishment
Name	Address	ID/FEI	Business Operations
Renu Laboratories, Inc.		945739449	manufacture(76348-409)