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NDC 11673-0062-15 Jock Itch 10 mg/g Details

Jock Itch 10 mg/g

Jock Itch is a TOPICAL CREAM in the HUMAN OTC DRUG category. It is labeled and distributed by TARGET Corporation. The primary component is CLOTRIMAZOLE.

MedlinePlus Drug Summary

Topical clotrimazole is used to treat tinea corporis (ringworm; fungal skin infection that causes a red scaly rash on different parts of the body), tinea cruris (jock itch; fungal infection of the skin in the groin or buttocks), and tinea pedis (athlete's foot; fungal infection of the skin on the feet and between the toes). Clotrimazole is in a class of antifungal medications called imidazoles. It works by stopping the growth of fungi that cause infection.

Related Packages: 11673-0062-15
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Clotrimazole Topical

Product Information

NDC	11673-0062
Product ID	11673-062_548504ca-cf9c-4316-9154-47fe51c42397
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Jock Itch
Proprietary Name Suffix	n/a
Non-Proprietary Name	Clotrimazole
Product Type	HUMAN OTC DRUG
Dosage Form	CREAM
Route	TOPICAL
Active Ingredient Strength	10
Active Ingredient Units	mg/g
Substance Name	CLOTRIMAZOLE
Labeler Name	TARGET Corporation
Pharmaceutical Class	Azole Antifungal [EPC], Azoles [CS]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part333C
Listing Certified Through	2024-12-31

Package

Package Images

NDC 11673-0062-15 (11673006215)

Pricing Information	N/A
NDC Package Code	11673-062-15
Billing NDC	11673006215
Package	1 TUBE in 1 CARTON (11673-062-15) / 14.2 g in 1 TUBE
Marketing Start Date	2020-04-27
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 1ae551e7-69de-4eef-b4f7-5e1a880e631d Details

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Clotrimazole 1%

Purpose

Antifungal

Uses

cures most jock itch
relieves itching, burning, scaling, chafing and discomfort associated with jock itch

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
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.

Directions

wash affected area and dry thoroughly
apply 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

Other information

To open: unscrew cap, use the pointed end of cap to puncture seal.
store between 20° - 25°C (68° - 77°F)
see carton or tube crimp for lot number and expiration date

Inactive ingredients

benzyl alcohol (1%), cetostearyl alcohol, cetyl esters wax, 2-octyldodecanol, polysorbate 60, purified water, sorbitan monostearate

Questions?

Call 1-866-923-4914

SPL UNCLASSIFIED SECTION

Distributed by

Target Corporation

Minneapolis,

MN 55403

PRINCIPAL DISPLAY PANEL - 14.2 g Tube Carton

up & up™

Compare to active ingredient in Lotrimin® AF*

jock itch cream

clotrimazole cream USP, 1% antifungal cream

cures most jock itch

relieves itching, burning, scaling and chafing

NET WT ½ OZ (14.2 g)

PRINCIPAL DISPLAY PANEL - 14.2 g Tube Carton

INGREDIENTS AND APPEARANCE

JOCK ITCH

clotrimazole cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:11673-062
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Clotrimazole (UNII: G07GZ97H65) (Clotrimazole - UNII:G07GZ97H65)	Clotrimazole	10 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
benzyl alcohol (UNII: LKG8494WBH)
cetostearyl alcohol (UNII: 2DMT128M1S)
cetyl esters wax (UNII: D072FFP9GU)
octyldodecanol (UNII: 461N1O614Y)
polysorbate 60 (UNII: CAL22UVI4M)
water (UNII: 059QF0KO0R)
sorbitan monostearate (UNII: NVZ4I0H58X)

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:11673-062-15	1 in 1 CARTON	04/27/2020
1		14.2 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH FINAL	part333C	04/27/2019

Labeler - TARGET Corporation (006961700)

Revised: 4/2020

Document Id: 548504ca-cf9c-4316-9154-47fe51c42397

Set id: 1ae551e7-69de-4eef-b4f7-5e1a880e631d

Version: 2

Effective Time: 20200430

Search by Drug Name or NDC

NDC 11673-0062-15 Jock Itch 10 mg/g Details

Jock Itch 10 mg/g

MedlinePlus Drug Summary

Product Information

Package

Package Images

NDC 11673-0062-15 (11673006215)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL 1ae551e7-69de-4eef-b4f7-5e1a880e631d Details

SPL UNCLASSIFIED SECTION

Active ingredient

Purpose

Uses

Warnings

Stop use and ask a doctor if

Directions

Other information

Inactive ingredients

Questions?

SPL UNCLASSIFIED SECTION

PRINCIPAL DISPLAY PANEL - 14.2 g Tube Carton

INGREDIENTS AND APPEARANCE

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