Initial Drug Listing-Tagrid Jock Itch Spray Tolnaftate 1%

Manufacturer: TAGRID LLC
Effective date: 2025-05-21
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: weekly-update
Hydrated at: 2026-07-17 21:43:15

Label at a glance#

ProductTagrid Jock Itch

Active ingredientTOLNAFTATE

Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate

OTC - PURPOSE SECTION

Antifungal

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

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

OTC - DO NOT USE SECTION

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

OTC - WHEN USING SECTION

OTC - STOP USE SECTION

Stop use and ask a doctor

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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

DOSAGE & ADMINISTRATION SECTION

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

OTC - QUESTIONS SECTION

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

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

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

jock itch.jpg

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0860013954741	GTIN-13: 0860013954741 EAN-13: 0860013954741 GTIN-12: 860013954741 UPC-A: 860013954741 GTIN storage (14 digits): 00860013954741	jock_itch.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

Tagrid Jock Itch
Tolnaftate
GLYCERIN
PHENOXYETHANOL
PEG-40 HYDROGENATED CASTOR OIL
POLYSORBATE 80
POLYSORBATE 20
SODIUM CITRATE
CITRIC ACID
WATER
ALCOHOL
PROPYLENE GLYCOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
85384-0009	85384-0009-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
TOLNAFTATE	06KB629TKV	ACTIB
GLYCERIN	PDC6A3C0OX	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
PEG-40 HYDROGENATED CASTOR OIL	7YC686GQ8F	IACT
POLYSORBATE 80	6OZP39ZG8H	IACT
POLYSORBATE 20	7T1F30V5YH	IACT
SODIUM CITRATE	1Q73Q2JULR	IACT
CITRIC ACID	2968PHW8QP	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
2	2025-05-21	full-release	2026-06-01 01:35:45

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Tagrid Jock Itch	TOLNAFTATE	TAGRID LLC	35a98b0c-9558-a464-e063-6294a90ab73e	2025-05-21	Warnings	Exact identifier ndc (package): 85384-0009-1 ndc (product): 85384-0009 ndc11 (package): 85384000901 spl id: 6b8ab7fc-1760-4dbc-9464-b2363bafb81e spl set id: 35a98b0c-9558-a464-e063-6294a90ab73e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.