DG HEALTH FEMININE ANTI-ITCH- benzocaine resorcinol cream

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)

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

DG HEALTH FEMININE ANTI-ITCH
benzocaine resorcinol cream

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
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)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM SULFITE (UNII: VTK01UQK3G)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
LANOLIN (UNII: 7EV65EAW6H)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ISOPROPYL STEARATE (UNII: 43253ZW1MZ)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC: 55910-158-28	28 g in 1 TUBE; Type 0: Not a Combination Product	06/13/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part348	06/13/2019

Labeler - DOLGENCORP, LLC (068331990)

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