UP AND UP ANTIFUNGAL- tolnaftate 1% cream

Up and Up Antifungal by

Drug Labeling and Warnings

Up and Up Antifungal by is a Otc medication manufactured, distributed, or labeled by Target Corporation, Sheffield Pharmaceuticals LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS 

Active ingredient

Tolnaftate 1%

Purpose 

Antifungal 

Uses

• for effective treatment of most athlete's foot (tinea pedis), jock itch (tinea cruris) and ringworm (tinea corporis)
• for effective relief of itchy, scaly skin between the toes
• clears up most athlete's foot infection and with daily use helps keep it from coming back

Warnings

For external use only

Do not use

• on children under 2 years of age unless directed by a doctor

When using this product avoid contact with eyes

Stop use and ask a doctor if

• irritation occurs or if there is no improvement within 4 weeks (for athlete's foot and ringworm)
• irritation occurs or if there is no improvement within 2 weeks (for jock itch)

Keep this and all drugs out of the reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

• clean the affected area and dry thoroughly
• apply a thin layer of the product over the 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

• use daily for 4 weeks. If condition persists longer, consult a doctor
• pay special attention to the spaces between the toes
• wear well fitting ventilated shoes
• change shoes and socks at least once daily

For ringworm, use daily for 4 weeks. If condition persists longer, consult a doctor.
For jock itch, use daily for 2 weeks. If condition persists longer, consult a doctor.
This product is not effective on the scalp or nails.

Other information 

store at controlled room temperature 20° -25°C (68-77°F)

Inactive ingredients

Ceteth-20, Cetostearyl Alcohol, Chlorocresol, Mineral Oil, Petrolatum , Propylene Glycol, Sodium Phosphate Monobasic, Water (Purified)

Questions or comments? call 1-800-910-6874

Principal display panel

Up &Up                NDC: 82442-020-28

Antifungal Cream 

Tolnaftate 1%

NET WT 1 OZ (28g)

INGREDIENTS AND APPEARANCE

UP AND UP ANTIFUNGAL 
tolnaftate 1% cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82442-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Tolnaftate (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV)	Tolnaftate	10 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
CETETH-20 (UNII: I835H2IHHX)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CHLOROCRESOL (UNII: 36W53O7109)
MINERAL OIL (UNII: T5L8T28FGP)
PETROLATUM (UNII: 4T6H12BN9U)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS (UNII: KH7I04HPUU)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82442-020-28	1 in 1 CARTON	08/01/2024
1		28 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	08/01/2024

Labeler - Target Corporation (006961700)

Registrant - Sheffield Pharmaceuticals LLC (151177797)

Establishment
Name	Address	ID/FEI	Business Operations
Sheffield Pharmaceuticals LLC		151177797	manufacture(82442-020) , analysis(82442-020)