Label: JINHWAGWANGSU BUBBLE- stearic acid soap
- 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.
Updated June 1, 2015
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- ACTIVE INGREDIENT
- INDICATIONS & USAGE
DOSAGE & ADMINISTRATION
Rub against the soap until bubbles appear and gently massage all over the skin and rinse off with water.
The soap contains moisturizing agents so it will easily become runny if it comes in contact with water. Keep it
away from water after use.
Hand-made soap may collect water bubbles on its surface if the air is humid, as the moisture in soap meets humidity and expanding. This is a natural phenomenon, so do not be concerned.
For external use only.
Do not eat, and do not use for purposes other than for skin cleansing.
Do not use on areas with wound, eczema, dermatitis...etc.
Immediately stop using in case of problems such as redness, swelling, itchiness, irritation…etc.
Immediately rinse with clean water if product gets in eyes.
Store away from UV rays.
- KEEP OUT OF REACH OF CHILDREN
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
stearic acid soap
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69871-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength STEARIC ACID (UNII: 4ELV7Z65AP) (STEARIC ACID - UNII:4ELV7Z65AP) STEARIC ACID 120 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) MYRISTIC ACID (UNII: 0I3V7S25AW) LAURIC ACID (UNII: 1160N9NU9U) TROLAMINE (UNII: 9O3K93S3TK) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) BENTONITE (UNII: A3N5ZCN45C) CHRYSANTHEMUM X MORIFOLIUM FLOWER (UNII: 2GR3C1A0WV) CASTOR OIL (UNII: D5340Y2I9G) EVENING PRIMROSE OIL (UNII: 3Q9L08K71N) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69871-001-01 100 g in 1 PACKAGE; Type 0: Not a Combination Product 06/01/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/01/2015 Labeler - CPbio Co., Ltd (689514410) Registrant - CPbio Co., Ltd (689514410) Establishment Name Address ID/FEI Business Operations CPbio Co., Ltd 689514410 manufacture(69871-001)