Search by Drug Name or NDC

NDC 49035-0253-21 Equate Jock Itch 10 mg/g Details

Equate Jock Itch 10 mg/g

Equate Jock Itch is a TOPICAL CREAM in the HUMAN OTC DRUG category. It is labeled and distributed by WALMART STORES INC. 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: 49035-0253-21
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Clotrimazole Topical

Product Information

NDC	49035-0253
Product ID	49035-253_3ba229d0-b0cd-4aa4-b1f1-c81b17a743ed
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	Equate 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	WALMART STORES INC
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 49035-0253-21 (49035025321)

Pricing Information	N/A
NDC Package Code	49035-253-21
Billing NDC	49035025321
Package	1 TUBE in 1 CARTON (49035-253-21) / 14.2 g in 1 TUBE
Marketing Start Date	2016-08-31
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 179141aa-b416-40bd-ab82-449f832dcac3 Details

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Clotrimazole USP 1% w/w

Purpose

Antifungal Cream

Uses

Cures athlete's foot (tinea pedis), jock itch (tinea cruris), ringworm (tinea corporis). Relieves the itching, irritation, redness, scaling and chafing associated with jock itch.

Warnings

Do not use on children under 2 years of age unless directed by a doctor.
For external use only.
Avoid contact with eyes.

Stop Use and ask a doctor

if irritation occurs or if there is no improvement within two weeks.

Keep this and all drugs out of the reach of children.

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

Directions

<This product is not effective on the scalp or nails.

Clean the affected area and dry thoroughly.
Apply a thin layer of this product over affected area twice daily (morning and night), or as directed by a doctor.
Supervise children in the use of this product.
use daily for 2 weeks.
If conditions persists longer, consult a doctor.>

Other information

Store at controlled room temperature 20°-25°C (68°-77°F).
Close cap tightly after use.

Inactive ingredients

aloe vera, benzyl alcohol, cetearyl alcohol, 2-octyldodecanol, polysorbate 60, sorbitan monostearate, spermwax, vitamin E, water

Questions?

For Questions or comments or to report an undesired reaction or side effect, please call 1-888-287-1915

Principal Display Panel – 1 oz. Tube

Equate Jock Itch NDC 49035-253-21

CLOTRIMAZOLE ANTI-FUNGAL CREAM

CREAM USP, 1%

Cures Most Athlete's Foot NET WT. 0.5oz ( 14.2 g)

Principal Display Panel – 0.5 oz. Carton

Equate Jock Itch NDC 49035-253-21

Cures Most

Athlete's Foot

Relieves Itching, Burning, Scaling, Discomfort and Chafing

CLOTRIMAZOLE ANTI-FUNGAL CREAM

CREAM USP, 1%

*Compare To the active ingredient in Lotrimin-AF®

NET WT. 0.5oz (14.2g)

Principal Display Panel – 0.5 oz. Carton

INGREDIENTS AND APPEARANCE

EQUATE JOCK ITCH

clotrimazole cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:49035-253
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
WATER (UNII: 059QF0KO0R)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
POLYSORBATE 60 (UNII: CAL22UVI4M)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
OCTYLDODECANOL (UNII: 461N1O614Y)
CETYL PALMITATE (UNII: 5ZA2S6B08X)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:49035-253-21	1 in 1 CARTON	08/31/2016
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	08/31/2016

Labeler - WALMART STORES INC (051957769)

Registrant - Sheffield Pharmaceuticals LLC (151177797)

Name	Address	ID/FEI	Business Operations
Establishment
Sheffield Pharmaceuticals LLC		151177797	MANUFACTURE(49035-253)

Revised: 8/2017

Document Id: 3ba229d0-b0cd-4aa4-b1f1-c81b17a743ed

Set id: 179141aa-b416-40bd-ab82-449f832dcac3

Version: 1

Effective Time: 20170817