SUNFLOWER

FDA Drug Profile — OrgaPlus Super Care Balm for combination and oi ly skin type 20g, OrgaPlus Super Care Balm for combination and oi ly skin type 14g

SUNFLOWER is listed in the FDA National Drug Code directory with 2 NDC codes, marketed under brand names including OrgaPlus Super Care Balm for combination and oi ly skin type 20g, OrgaPlus Super Care Balm for combination and oi ly skin type 14g. Available dosage form: stick.

Drug Details

Generic Name
SUNFLOWER
Brand Names
OrgaPlus Super Care Balm for combination and oi ly skin type 20g, OrgaPlus Super Care Balm for combination and oi ly skin type 14g
Application Number
Sponsor
BLUEZONWIDE CO.,LTD
NDC Codes
2
Dosage Forms
STICK
Routes
TOPICAL
Active Ingredients
SUNFLOWER OIL

Indications and Usage

Indications & Usage ■ temporarily protects minor ■ rashes ■ blisters ■ helps prevent and temporarily protects and helps relieve ■ cracked skin ■ temporarily protects and helps relieve minor skin irritation and itching due to ■ poison ivy ■ poison sumac ■ poison oak ■ temporarily protects and helps relieve minor pain associated with ■ poison ivy ■ poison sumac ■ poison oak

Warnings

Warnings Section Warnings For external use only. ■ Do not use on ■ on deep wounds ■ animal bites ■ serious burns ■ Stop use and ask a doctor if ■ condition worsens ■ symptoms last more than 7 days or clear up and occur again within a few days ■ When using this product keep out of eyes. Rinse with water to remove.