Label: SOME BY MI AHA BHA PHA 30 DAYS MIRACLE ACNE BODY CLEANSER cream
- NDC Code(s): 74472-102-01
- Packager: PERENNEBELL Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 13, 2023
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- ACTIVE INGREDIENT
- INDICATIONS & USAGE
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WARNINGS
For external use only
When using this product ■ skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. - KEEP OUT OF REACH OF CHILDREN
- WHEN USING
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INACTIVE INGREDIENT
Water, Lauric Acid, Glycerin, Potassium Hydroxide, Myristic Acid, Sodium Chloride, Sodium C14-16 Olefin Sulfonate, Lauryl Hydroxysultaine, Benzyl Glycol, Coco-Betaine, Butylene Glycol, Ethylhexylglycerin, Melia Azadirachta Leaf Extract, Melaleuca Alternifolia [Tea Tree] Leaf Water, Centella Asiatica Extract, Asiaticoside, Madecassic Acid, Gluconolactone, Citric acid, Asiatic Acid, Mandelic Acid, Madecassoside, Artemisia Vulgaris Extract, Disodium EDTA, Coptis Japonica Root Extract, 1,2-Hexanediol, Melia Azadirachta Flower Extract, Eucalyptus Globulus Leaf Oil, Ethyl Hexanediol
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OTHER SAFETY INFORMATION
■ Sunburn Alert: This product contains an alpha hydroxy acid [AHA] that may increase your skin's sensitivity to the sun and particularly the possibility of sunburn. Use a sunscreen, wear protective clothing, and limit sun exposure while using this product and for a week afterwards.
■Test any product that contains a BHA on a small area of skin before applying it to a large area. If you use cosmetics with BHAS and experience skin irritation or prolonged stinging, stop using the product and consult your physician.
SUNBURN ALERT
- DOSAGE & ADMINISTRATION
- PURPOSE
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INSTRUCTIONS FOR USE
■Clean the skin thoroughly before applying this product.
■Take an appropriate amount and foam enough on your face then wash off with water.
■Because excessive drying of the skin may occur, start with one application daily, then gradually increase if needed or as directed by a doctor.■If bothersome dryness or peeling occurs, reduce application to once a day or every other day.
■ Avoid using BHA-containing products on infants and children.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SOME BY MI AHA BHA PHA 30 DAYS MIRACLE ACNE BODY CLEANSER
some by mi aha bha pha 30 days miracle acne body cleanser creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74472-102 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g in 400 g Inactive Ingredients Ingredient Name Strength LAURIC ACID (UNII: 1160N9NU9U) GLYCERIN (UNII: PDC6A3C0OX) SODIUM CHLORIDE (UNII: 451W47IQ8X) LAURYL HYDROXYSULTAINE (UNII: 176KKP31OZ) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) COPTIS JAPONICA ROOT (UNII: JH0SWT16D1) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) AZADIRACHTA INDICA FLOWER (UNII: 3TE8A92UPM) CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J) MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL (UNII: VIF565UC2G) ASIATICOSIDE (UNII: PKO39VY215) MADECASSIC ACID (UNII: M7O1N24J82) ETHYLENE GLYCOL MONOBENZYL ETHER (UNII: 06S8147L47) WATER (UNII: 059QF0KO0R) AZADIRACHTA INDICA LEAF (UNII: HKY915780T) ETHOHEXADIOL (UNII: M9JGK7U88V) MADECASSOSIDE (UNII: CQ2F5O6YIY) MANDELIC ACID (UNII: NH496X0UJX) GLUCONOLACTONE (UNII: WQ29KQ9POT) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) ASIATIC ACID (UNII: 9PA5A687X5) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) COCO-BETAINE (UNII: 03DH2IZ3FY) EUCALYPTUS OIL (UNII: 2R04ONI662) MYRISTIC ACID (UNII: 0I3V7S25AW) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) Product Characteristics Color green Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74472-102-01 1 in 1 BOX 12/15/2023 1 1 g in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 12/05/2023 Labeler - PERENNEBELL Co., Ltd. (694788814) Establishment Name Address ID/FEI Business Operations reBom Co., Ltd. 695951708 manufacture(74472-102)