Label: SANDAWHA NATURAL MILD CLEANSING OIL- camellia japonica seed oil liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 72289-0012-1 - Packager: SKINCURE INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated November 24, 2020
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Dongbakex
Camellia Japonica Flower Extract 28.0300
Camellia Japonica Seed Extract
Caprylic/Capric Triglyceride
Camellia Sinensis Seed Oil
Canola Oil 15.0000
Helianthus Annuus (Sunflower) Seed Oil 15.0000
Polyglyceryl-4 Oleate 14.0000
Ricinus Communis (Castor) Seed Oil 10.0000
Macadamia Integrifolia Seed Oil 1.0000
Olea Europaea (Olive) Fruit Oil 1.0000
Rosa Canina Fruit Oil 0.1000
MultiOil OilSoother
Olea Europaea (Olive) Fruit Oil 0.1000
Camellia Japonica Seed Oil
Tocopherol
Bisabolol
Rosa Canina Fruit Oil
Magnolia Kobus Bark Extract 0.0200
Citrus Limon (Lemon) Peel Oil 0.3750
Aniba Rosodora (Rosewood) Wood Oil 0.2250
Lavandula Angustifolia (Lavender) Oil 0.1500 - PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SANDAWHA NATURAL MILD CLEANSING OIL
camellia japonica seed oil liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72289-0012 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAMELLIA JAPONICA SEED OIL (UNII: U37N0S910T) (CAMELLIA JAPONICA SEED OIL - UNII:U37N0S910T) CAMELLIA JAPONICA SEED OIL 15 g in 100 mL Inactive Ingredients Ingredient Name Strength CANOLA OIL (UNII: 331KBJ17RK) ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72289-0012-1 200 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/23/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 11/23/2020 Labeler - SKINCURE INC (557830240) Registrant - SKINCURE INC (557830240) Establishment Name Address ID/FEI Business Operations SKINCURE INC 557830240 label(72289-0012) , manufacture(72289-0012)