74472-005 Some by Mi Aha-Bha-Pha 30 Days Miracle Serum Light
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SOME BY MI AHA BHA PHA 30 DAYS MIRACLE SERUM LIGHT- salicylic acid liquid PERENNEBELL Co., Ltd. Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies. ---------- 74472-005_SOME BY MI AHA-BHA-PHA 30 DAYS MIRACLE SERUM LIGHT Salicylic Acid 0.005% Acne Treatment For the treatment of Acne After lightly shaking the product, apply I following the skin texture using fingertip. After applying the product, cover your face with hand for better absorption. 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. avoid contact with eyes. If contact occurs, flush thoroughly with water. People with allergy to aspirin will react poorly to the Salicylic Acid. Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away. Melaleuca Alternifolia (Tea Tree) Leaf Water, Centella Asiatica Extract, Dipropylene Glycol, Niacinamide Houttuynia Cordata Extract, Artemisia Princeps Leaf Extract, Centella Asiatica Leaf Extract, Madecassoside, Madecassic Acid, Asiaticoside, Asiatic Acid, Melia Azadirachta Leaf Extract, Melia Azadirachta Flower Extract, Salix Alba (Willow) Bark Extract, Pimpinella Anisum (Anise) Fruit Extract, Scutellaria Baicalensis Root Extract, Glycerin, Butylene Glycol, Hydroxyethyl Urea, Allantoin, Panthenol, Sodium Hyaluronate, Adenosine, Arginine, Tremella Fuciformis Polysaccharide, Lactobionic Acid, Citric Acid, C12-13 Pareth-9, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Xanthan Gum, Sclerotium Gum, Algin, Water, 1,2-Hexanediol, Benzyl Glycol, Ethylhexylglycerin, Raspberry Ketone, Disodium EDTA, Mentha Piperita (Peppermint) Oil SOME BY MI AHA BHA PHA 30 DAYS MIRACLE SERUM LIGHT salicylic acid liquid Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74472-005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ 4LPZ ) (SALICYLIC ACID - UNII:O414PZ 4LPZ ) SALICYLIC ACID 0.005 g in 100 mL Inactive Ingredients Ingredient Name Strength TEA TREE OIL (UNII: VIF565UC2G) CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U) DIPROPYLENE GLYCOL (UNII: E107L85C40) NIACINAMIDE (UNII: 25X51I8RD4) HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ 22) ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G) CENTELLA ASIATICA LEAF (UNII: 6810070TYD) MADECASSOSIDE (UNII: CQ2F5O6YIY) MADECASSIC ACID (UNII: M7O1N24J82) ASIATICOSIDE (UNII: PKO39VY215) ASIATIC ACID (UNII: 9PA5A687X5) AZADIRACHTA INDICA LEAF (UNII: HKY915780T) AZADIRACHTA INDICA FLOWER (UNII: 3TE8A92UPM) SALIX ALBA BARK (UNII: 205MXS71H7) ANISE (UNII: 21C2F5E8RE) SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) GLYCERIN (UNII: PDC6A3C0OX) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR) ALLANTOIN (UNII: 344S277G0Z ) PANTHENOL (UNII: WV9CM0O67Z ) HYALURONATE SODIUM (UNII: YSE9PPT4TH) ADENOSINE (UNII: K72T3FS567) ARGININE (UNII: 94Z LA3W45F) LACTOBIONIC ACID (UNII: 65R938S4DV) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) C12-13 PARETH-9 (UNII: 9BXD858P37) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) XANTHAN GUM (UNII: TTV12P4NEE) BETASIZOFIRAN (UNII: 2X51AD1X3T) SODIUM ALGINATE (UNII: C269C4G2Z Q) WATER (UNII: 059QF0KO0R) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) ETHYLENE GLYCOL MONOBENZYL ETHER (UNII: 06S8147L47) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) 4-(P-HYDROXYPHENYL)-2-BUTANONE (UNII: 7QY1MH15BG) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) PEPPERMINT OIL (UNII: AV092KU4JH) Packaging Marketing Start Marketing End # Item Code Package Description Date Date NDC:74472-005- 1 1 in 1 CARTON 03/17/2021 02 NDC:74472-005- 50 mL in 1 BOTTLE; Type 0: Not a Combination 1 01 Product Marketing Information Marketing Application Number or Monograph Marketing Start Marketing End Category Citation Date Date OTC monograph final part333D 03/17/2021 Labeler - PERENNEBELL Co., Ltd. (694788814) Registrant - PERENNEBELL Co., Ltd. (694788814) Establishment Name Address ID/FEI Business Operations reBom Co., Ltd. 688733595 manufacture(74472-005) Revised: 3/2021 PERENNEBELL Co., Ltd..