HEB  ANTIFUNGAL- clotrimazole cream 
H E B

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.

----------

HEB®
Antifungal

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 4 weeks (for athlete's foot or ringworm) or 2 weeks (for jock itch)

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

PRINCIPAL DISPLAY PANEL - 14.2 g Tube Carton

Compare to Lotrimin® AF* active ingredient

NDC 37808-305-01

H-E-B®
Athlete's Foot Cream
Clotrimazole Cream USP, 1%
Antifungal

Cures Most
Athlete's Foot

• Relieves Itching, Burning, Cracking and Scaling
NET WT. 0.5 OZ (14.2g)

PRINCIPAL DISPLAY PANEL - 14.2 g Tube Carton
HEB   ANTIFUNGAL
clotrimazole cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-305
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37808-305-011 in 1 CARTON08/31/1993
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 - H E B (007924756)
Registrant - Taro Pharmaceuticals U.S.A., Inc. (145186370)
Establishment
NameAddressID/FEIBusiness Operations
Taro Pharmaceuticals Inc.206263295MANUFACTURE(37808-305)

Revised: 3/2019
Document Id: a5b96d51-97c1-44a9-80d1-e20347329e8f
Set id: 8f07dc5a-cfa8-4a57-ac90-552a7c947cc5
Version: 3
Effective Time: 20190307
 
H E B