Drug Facts Active ingredients

Benzocaine 20%

Resorcinol 3%

Purpose

External analgesic

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.

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)

Directions

adults and children 2 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 2 years	do not use; consult a doctor

Other Information

store at 20° -25° C (68° -77° F)

Inactive Ingredients

acrylates/C10-30 alkyl acrylate, crosspolymer (60000 mPa.s), aloe barbadensis leaf juice, aminomethylpropanol, cetyl alcohol, corn oil, glyceryl stearate, isopropyl myristate, isopropyl palmitate, lanolin, methylparaben, PEG-100 stearate, potassium cetyl phosphate, propylene glycol, sodium sulfite, tocopheryl acetate, trisodium HEDTA, vitamin A palmitate, vitamin D3, water

Questions or comments?

1-866-326-1313

HealthWise Maximum Strength Feminine Anti-Itch Cream, 1oz

label

HEALTHWISE FEMININE ANTI-ITCH CREAM
benzocaine, resorcinol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71101-066
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	20 g in 100 g
RESORCINOL (UNII: YUL4LO94HK) (RESORCINOL - UNII:YUL4LO94HK)	RESORCINOL	3 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TRISODIUM HEDTA (UNII: K3E0U7O8KI)
CETYL ALCOHOL (UNII: 936JST6JCN)
CHOLECALCIFEROL (UNII: 1C6V77QF41)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
CORN OIL (UNII: 8470G57WFM)
LANOLIN (UNII: 7EV65EAW6H)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
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)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
METHYLPARABEN (UNII: A2I8C7HI9T)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:71101-066-01	28.3 g in 1 TUBE; Type 0: Not a Combination Product	04/01/2026

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M017	04/01/2026

Labeler - Veridian Healthcare (830437997)