DG HEALTH FEMININE ANTI-ITCH- benzocaine resorcinol cream 
DOLGENCORP, LLC

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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Drug Facts

Active ingredients

Benzocaine 20%

Resorcinol 3%

Purpose

External analgesic

External analgesic

Use

temporarily relieves itching

Warnings

For external use only

Avoid contact with eyes

Stop use and ask a doctor if

condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days

Do not apply over large areas of the body

Do not use

Do not apply over large areas of the body

Do not use if allergic to any of the ingredients

Keep out of reach of children

If swallowed get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Directions

adults and children 12 years and older: Apply a fingertip amount (approximately 1-inch strip) to affected area not more than 3 to 4 times daily. Clean nozzle of tube by wiping thoroughly before replacing cap. Keep cap tightly closed between uses

children under 12 years of age: Consult a doctor

Inactive ingredients

aloe barbadensis leaf extract, carbomer, cetyl alcohol, cholecalciferol, glyceryl stearate, isopropyl myristate, isopropyl palmitate, isopropyl stearate, lanolin, methylparaben, mineral oil, PEG-100 stearate, propylene glycol, retinyl palmitate, sodium hydroxide, sodium sulfite, tocopheryl acetate, trisodium HEDTA, water

Questions or comments?

1-888-309-9030

Package Label

Package Label

DG HEALTH  FEMININE ANTI-ITCH
benzocaine resorcinol cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55910-158
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE20 g  in 100 g
RESORCINOL (UNII: YUL4LO94HK) (RESORCINOL - UNII:YUL4LO94HK) RESORCINOL3 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
MINERAL OIL (UNII: T5L8T28FGP)  
TRISODIUM HEDTA MONOHYDRATE (UNII: 463A7RIB6K)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
PEG-100 STEARATE (UNII: YD01N1999R)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
CHOLECALCIFEROL (UNII: 1C6V77QF41)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SODIUM SULFITE (UNII: VTK01UQK3G)  
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
LANOLIN (UNII: 7EV65EAW6H)  
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ISOPROPYL STEARATE (UNII: 43253ZW1MZ)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55910-158-2828 g in 1 TUBE; Type 0: Not a Combination Product06/13/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34806/13/2019
Labeler - DOLGENCORP, LLC (068331990)

Revised: 9/2023
 
DOLGENCORP, LLC