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NDC 00363-0695-90 jock itch 1 g/100g Details

jock itch 1 g/100g

jock itch is a TOPICAL SPRAY in the HUMAN OTC DRUG category. It is labeled and distributed by Walgreen Company. The primary component is TOLNAFTATE.

MedlinePlus Drug Summary

Tolnaftate stops the growth of fungi that cause skin infections, including athlete's foot, jock itch, and ringworm. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Related Packages: 00363-0695-90
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Tolnaftate

Product Information

NDC	00363-0695
Product ID	0363-0695_ae539fc7-1fa6-48d3-8de8-88c30699d6b3
Associated GPIs	90150085003305
GCN Sequence Number	007336
GCN Sequence Number Description	tolnaftate AERO POWD 1 % TOPICAL
HIC3	Q5F
HIC3 Description	TOPICAL ANTIFUNGALS
GCN	30290
HICL Sequence Number	003186
HICL Sequence Number Description	TOLNAFTATE
Brand/Generic	Generic
Proprietary Name	jock itch
Proprietary Name Suffix	n/a
Non-Proprietary Name	Tolnaftate
Product Type	HUMAN OTC DRUG
Dosage Form	SPRAY
Route	TOPICAL
Active Ingredient Strength	1
Active Ingredient Units	g/100g
Substance Name	TOLNAFTATE
Labeler Name	Walgreen Company
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part333C
Listing Certified Through	2024-12-31

Package

Package Images

NDC 00363-0695-90 (00363069590)

Pricing Information	N/A
NDC Package Code	0363-0695-90
Billing NDC	00363069590
Package	130 g in 1 CAN (0363-0695-90)
Marketing Start Date	2005-06-08
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL c86ab353-75fb-496c-a812-04a0679edaf7 Details

Active ingredient

Tolnaftate 1%

Purpose

Antifungal

Uses

•: cures most jock itch
•: for effective relief of itching, chafing and burning

Warnings

For external use only

Flammable: Do not use while smoking or near heat or flame

Do not use

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

When using this product

•: avoid contact with the eyes
•: use only as directed. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.
•: contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120°F (49°C).

Stop use and ask a doctor if

•: irritation occurs
•: there is no improvement within 2 weeks

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Directions

•: wash affected area and dry thoroughly
•: shake can well and spray a thin layer over affected area twice daily (morning and night)
•: supervise children in the use of this product
•: use daily for 2 weeks; if condition persists longer, ask a doctor
•: this product is not effective on the scalp or nails
•: in case of clogging, clean nozzle with a pin

Other information

•: store at 20-25°C (68-77°F)

Inactive ingredients

alcohol denat., aluminum starch octenylsuccinate, isobutane, isopropyl myristate, propylene carbonate, sorbitan monooleate, stearalkonium hectorite, talc

Questions or comments?

1-800-719-9260

Package/Label Principal Display Panel

Compare to Tinactin® active ingredient

Jock Itch Powder Spray

TOLNAFTATE 1% / ANTIFUNGAL

MAXIMUM STRENGTH

Cures most jock itch

Soothes & relieves itching, burning & chafing

NET WT 4.6 OZ (130 g)

INGREDIENTS AND APPEARANCE

JOCK ITCH

tolnaftate spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0363-0695
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV)	TOLNAFTATE	1 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
ALCOHOL (UNII: 3K9958V90M)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
ISOBUTANE (UNII: BXR49TP611)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
STEARALKONIUM HECTORITE (UNII: OLX698AH5P)
TALC (UNII: 7SEV7J4R1U)

Product Characteristics
Color	WHITE (off-white)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0363-0695-90	130 g in 1 CAN; Type 0: Not a Combination Product	06/08/2005

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333C	06/08/2005

Labeler - Walgreen Company (008965063)

Revised: 10/2020

Document Id: ae539fc7-1fa6-48d3-8de8-88c30699d6b3

Set id: c86ab353-75fb-496c-a812-04a0679edaf7

Version: 6

Effective Time: 20201013