FDA Label for Neutrogena Sun Rescue After Sun Medicated Relief
View Indications, Usage & Precautions
Neutrogena Sun Rescue After Sun Medicated Relief Product Label
The following document was submitted to the FDA by the labeler of this product Johnson & Johnson Consumer 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.
Other
Drug Facts
Distributed by:
JOHNSON & JOHNSON CONSUMER INC.
Skillman, NJ 08558
Active Ingredient
Camphor 0.45%
Purpose
External analgesic
Use
temporarily relieves pain and itching associated with sunburn
Warnings
For external use only.
Flammable: Keep away from fire or flame
Otc - When Using
When using this product avoid contact with eyes
Stop Use And Ask A Doctor If
- condition worsens
- symptoms persist for more than 7 days or clear up and occur again within a few days
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 2 years of age and older: apply to affected area not more than 3 to 4 times daily
- children under 2 years of age: ask a doctor
Other Information
- Store at 20° to 25°C (68° to 77°F)
Inactive Ingredients
Water, Alcohol Denat., Triethanolamine, Carbomer, EDTA
Questions?
Call toll-free 800-299-4786 or 215-273-8755 (collect) or visit www.neutrogena.com
Principal Display Panel - 85 G Tube Label
NEW
Neutrogena®
DERMATOLOGIST RECOMMENDED BRAND
NEUTROGENA®
SUN
RESCUE
AFTER SUN
MEDICATED RELIEF GEL
CAMPHOR EXTERNAL ANALGESIC
pain relief for sunburn
cools, calms and soothes
skin on contact
NET WT 3.0 OZ (85 g)
* Please review the disclaimer below.