TAGRID JOCK ITCH- tolnaftate spray

Tagrid Jock Itch by

Drug Labeling and Warnings

Tagrid Jock Itch by is a Otc medication manufactured, distributed, or labeled by TAGRID LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Tolnaftate

PURPOSE

Antifungal

INDICATIONS & USAGE

■ Cures and prevents most jock itch (tinea cruris)
■ Relieves itching, chafing, and irritation associated with jock itch
■ Helps prevent recurrence when used daily

WARNINGS

For external use only

Avoid contact with eyes, mouth, or mucous
membranes
Do not apply to broken or irritated skin
Flammable: Keep away from heat and flame

■ on children under 2 years of age unless directed by a doctor
■ for diaper rash

Stop use and ask a doctor

Condition worsens or does not improve within 2 weeks
Excessive irritation or burning occurs

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions
Clean the affected area and dry thoroughly.
Shake can well and spray a thin layer over affected area twice daily (morning and night).

Use daily for 2 weeks

OTHER SAFETY INFORMATION

Other Information
Store between 20°C to 25°C (68°F to 77°F)
Avoid excessive heat and direct sunlight
Protect from freezing
Do not puncture or incinerate the can

QUESTIONS

Questions or comments?
Contact us at:
support@tagridstore.com

Distributed by TAGRID LLC
San Francisco, CA, USA 94131
Website: tagridstore.com

INACTIVE INGREDIENT

Inactive Ingredients:
Alcohol, Propylene Glycol, PEG-40 Hydrogenated,Castor Oil, Polysorbate 20, Polysorbate 80, Glycerin,
Phenoxyethanol, Citric Acid, Sodium Citrate, Purified Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TAGRID JOCK ITCH 
tolnaftate spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85384-0009
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 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PEG-40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
CITRIC ACID (UNII: 2968PHW8QP)
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85384-0009-1	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/04/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	06/04/2025

Labeler - TAGRID LLC (118778969)