EQUALINE ANTIFUNGAL CREAM- clotrimazole cream 
SUPERVALU 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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Equaline Antifungal Cream 0.5oz Clotrimazole 1% 26369 ZDP

Active ingredient Purpose

Clotrimazole 1%..............................Antifungal

Uses

Warnings

For external use only

Do not use on children under 2 years of age except under the advice and supervision of a doctor.

When using this product, avoid contact with the eyes.

Stop use and ask a doctor if

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Other information

Inactive ingredients

cetosteryl alcohol, ethylparaben, glycerin, light mineral oil, propylene glycol, purified water, sodium sulfite, steareth-20,stearic acid

Distributed by:

UNFI

Providence, RI 02908 USA

Made in China

26369

EQUALINE ANTIFUNGAL CREAM 
clotrimazole cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-963
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
WATER (UNII: 059QF0KO0R)  
ETHYLPARABEN (UNII: 14255EXE39)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SODIUM SULFITE (UNII: VTK01UQK3G)  
LIGHT MINERAL OIL (UNII: N6K5787QVP)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
GLYCERIN (UNII: PDC6A3C0OX)  
STEARETH-20 (UNII: L0Q8IK9E08)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41163-963-141 in 1 CARTON10/06/2020
114 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C10/06/2020
Labeler - SUPERVALU INC (006961411)

Revised: 3/2022
Document Id: db8ab2f1-c086-adce-e053-2a95a90a0467
Set id: aa6af065-8dff-576a-e053-2a95a90a1d13
Version: 3
Effective Time: 20220331
 
SUPERVALU INC