FEMININE ANTI-ITCH CREME- benzocaine, resorcinol cream 
Quality Choice (CHAIN DRUG MARKETING ASSOCIATION)

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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Quality Choice Maximum Strength Feminine Anti-itch Cream

Drug Facts Active ingredients

Benzocaine 20%

Resorcinol 3%

Purpose

External analgesic

Keep out of reach of children

Keep out of reach of children.

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

Use

temporarily relieves itching

Warnings

For external use only

When using this product

avoid contact with the eyes

Stop use and ask a doctor if

condition worsens, or if symptoms persist for more than7 days or clear up and occur again within a few days

Do not apply Directions

Do not apply over large area of the body.

adults and children 12 years and older apply a fingertip amount (approximately 1-inch strip) to the affected area not more than 3 to 4 times daily

children under 12 years ask a doctor

Other Information

store at 20° -25° C (68° -77° F)

Inactive Ingredients

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


Questions or comments?

800-935-2362

Quality Choice Maximum Strength Feminine Anti-itch Cream

label

FEMININE ANTI-ITCH CREME 
benzocaine, resorcinol cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-949
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE5.67 g  in 28 g
RESORCINOL (UNII: YUL4LO94HK) (RESORCINOL - UNII:YUL4LO94HK) RESORCINOL0.85 g  in 28 g
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
CHOLECALCIFEROL (UNII: 1C6V77QF41)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
ISOPROPYL STEARATE (UNII: 43253ZW1MZ)  
LANOLIN (UNII: 7EV65EAW6H)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
MINERAL OIL (UNII: T5L8T28FGP)  
PEG-100 STEARATE (UNII: YD01N1999R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SODIUM SULFITE (UNII: VTK01UQK3G)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
TRISODIUM HEDTA (UNII: K3E0U7O8KI)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63868-949-0128 g in 1 TUBE; Type 0: Not a Combination Product02/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34802/01/2020
Labeler - Quality Choice (CHAIN DRUG MARKETING ASSOCIATION) (011920774)

Revised: 2/2023
Document Id: f5391ab7-dcf9-a88d-e053-2a95a90a5fa6
Set id: aa6cc963-dc60-5222-e053-2995a90acaf6
Version: 2
Effective Time: 20230221
 
Quality Choice (CHAIN DRUG MARKETING ASSOCIATION)