FDA Label for Rexall Feminine Maximum Strength Anti-itch
View Indications, Usage & Precautions
Rexall Feminine Maximum Strength Anti-itch Product Label
The following document was submitted to the FDA by the labeler of this product Dolgencorp, Inc.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredients
Benzocaine 20%
Resorcinol 3%
Purpose
External Analgesic
External Analgesic
Use
- Temporarily relieves itching
Warnings
For external use only
Otc - When Using
When using this product avoid contact with eyes
Otc - Stop Use
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. Also, do not use if you have an unusual or abnormal vaginal discharge except under the supervision of a physician.
Do not apply over large areas of the body.
Otc - 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.
Directions
adults and children 12 years and older
apply a fingertip amount (approximately 1-inch strip) to Tthe affected area not more than 3 to 4 times daily
children under 12 years
consult a doctor
Other Information
store at 20°-25°C (68°-77°F)
Inactive Ingredients
aloe vera gel, carbomer, cetyl alcohol, corn oil, disodium EDTA, fragrance, glyceryl stearate, isopropyl myristate, isopropyl palmitate, lanolin, methyl-4 hydroxybenzoate, mineral oil, PEG-100 stearate, propylene glycol, purified water, stearic acid, stearyl alcohol, triethanolamine, vitamin A, E & D
Principal Display Panel - 28 G Carton Label
REXALL FEMININE MAXIMUM STRENGTH ANTI-ITCH CREAM
NET WT 1 OZ (28 g)
* Please review the disclaimer below.
