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NDC 11673-0504-58 Up and Up Jock Itch Relief 1 g/100g Details

Up and Up Jock Itch Relief 1 g/100g

Up and Up Jock Itch Relief 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: 11673-0504-58
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Clotrimazole Topical

Product Information

NDC	11673-0504
Product ID	11673-504_9b77d64e-6226-4251-baa4-21f0eade6c36
Associated GPIs
GCN Sequence Number	007361
GCN Sequence Number Description	clotrimazole CREAM (G) 1 % TOPICAL
HIC3	Q5F
HIC3 Description	TOPICAL ANTIFUNGALS
GCN	30370
HICL Sequence Number	004137
HICL Sequence Number Description	CLOTRIMAZOLE
Brand/Generic	Generic
Proprietary Name	Up and Up Jock Itch Relief
Proprietary Name Suffix	n/a
Non-Proprietary Name	Clotrimazole
Product Type	HUMAN OTC DRUG
Dosage Form	CREAM
Route	TOPICAL
Active Ingredient Strength	1
Active Ingredient Units	g/100g
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 11673-0504-58 (11673050458)

Pricing Information	N/A
NDC Package Code	11673-504-58
Billing NDC	11673050458
Package	1 TUBE in 1 CARTON (11673-504-58) / 14 g in 1 TUBE
Marketing Start Date	2013-09-17
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL f53d5418-5878-4c86-a2bb-b0ff61aec768 Details

Active ingredient

Clotrimazole 1%

Purpose

Antifungal

Uses

•: cures most jock itch
•: relieves itching, burning, scaling, chafing and discomfort which accompany this condition

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 the 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 the 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

•: store at 20°-25°C (68°-77°F)

Inactive ingredients

benzyl alcohol, cetostearyl alcohol, cetyl esters wax, octyldodecanol, polysorbate 60, purified water, sorbitan monostearate

Questions?

Call 1-888-547-7400

Package/Label Principal Display Panel

Compare to active ingredient in Lotrimin®AF

jock itch relief

antifungal cream

clotrimazole 1%

cures most jock itch

relieves itching, burning, scaling and chafing

NET WT 0.5 OZ (14 g)

INGREDIENTS AND APPEARANCE

UP AND UP JOCK ITCH RELIEF

clotrimazole cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:11673-504
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CLOTRIMAZOLE (UNII: G07GZ97H65) (CLOTRIMAZOLE - UNII:G07GZ97H65)	CLOTRIMAZOLE	1 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
BENZYL ALCOHOL (UNII: LKG8494WBH)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETYL ESTERS WAX (UNII: D072FFP9GU)
POLYSORBATE 60 (UNII: CAL22UVI4M)
WATER (UNII: 059QF0KO0R)
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
OCTYLDODECANOL (UNII: 461N1O614Y)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:11673-504-58	1 in 1 CARTON	09/17/2013
1		14 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	09/17/2013

Labeler - Target Corporation (006961700)

Revised: 7/2016

Document Id: 9b77d64e-6226-4251-baa4-21f0eade6c36

Set id: f53d5418-5878-4c86-a2bb-b0ff61aec768

Version: 3

Effective Time: 20160708