SIGNATURE CARE  JOCK ITCH- clotrimazole cream 
Safeway Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Signature Care
Jock Itch

Drug Facts

Active ingredient

Clotrimazole 1%

Purpose

Antifungal

Uses

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

Other information

Inactive ingredients

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

Questions?

Call 1-866-923-4914

DISTRIBUTED BY BETTER LIVING BRANDS LLC
P.O. BOX 99, PLEASANTON, CA 94566-0009

PRINCIPAL DISPLAY PANEL - 14.2 g Tube Carton

Signature™
care
Quality
Guaranteed

Compare to
Lotrimin® AF
active ingredient*

NDC 21130-210-01

JOCK ITCH CREAM
CLOTRIMAZOLE CREAM USP, 1%

ANTIFUNGAL CREAM
RELIEVES ITCHING, BURNING, SCALING & CHAFING

NET WT (½ oz) 14.2 g

PRINCIPAL DISPLAY PANEL - 14.2 g Tube Carton
SIGNATURE CARE   JOCK ITCH
clotrimazole cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21130-210
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Clotrimazole (UNII: G07GZ97H65) (Clotrimazole - UNII:G07GZ97H65) Clotrimazole10 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
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
ColorWHITEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:21130-210-011 in 1 CARTON08/23/2019
114.2 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart333C08/31/1993
Labeler - Safeway Inc. (009137209)

Revised: 8/2019
Document Id: 1976eb4c-93fb-4c61-a05e-1a9d0089e81c
Set id: 9ec8b527-0f03-4433-8d33-635e746fdf79
Version: 2
Effective Time: 20190827
 
Safeway Inc.