Label: SURFREE KOJIC ACID- soap soap
- NDC Code(s): 83872-519-01
- Packager: Shenzhen Xiaomai Manufacturing Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 10, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
- Do not use
- When Using
-
Stop Use
"chest pain, rapid heart beat.faintness, or dizziness occurs sudden, unexplained weight gain occurs.
your hands or feet swell scalp imitation or redness occurs
May be harmful if used when pregnant or breast-feeding
Keep Out Of Reach Of Chlidren:
if swallowed,get medical help or
contact a Poison Control Center right away." - Ask Doctor
- Keep Out Of Reach Of Chlidren
-
Directions
1.Wet the skin: Moisten your face or body with warm water.
2.Lather the soap: Rub the soap to create foam.
3.Gently massage: Apply the foam to your skin and massage gently for 1-2 minutes, focusing on areas with dark spots or uneven tone.
3.Rinse thoroughly: Wash off with warm water to remove all the foam.
4.Moisturize: Apply a moisturizer afterward to lock in hydration and protect the skin barrier. - Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SURFREE KOJIC ACID
soap soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83872-519 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength KOJIC ACID (UNII: 6K23F1TT52) (KOJIC ACID - UNII:6K23F1TT52) KOJIC ACID 5 g in 260 g Inactive Ingredients Ingredient Name Strength AQUA (UNII: 059QF0KO0R) SHEA BUTTER (UNII: K49155WL9Y) GLYCERIN (UNII: PDC6A3C0OX) OLIVE OIL (UNII: 6UYK2W1W1E) SODIUM CHLORIDE (UNII: 451W47IQ8X) TURMERIC (UNII: 856YO1Z64F) FD&C RED NO. 3 (UNII: PN2ZH5LOQY) HYALURONIC ACID (UNII: S270N0TRQY) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) RETINOL (UNII: G2SH0XKK91) ASCORBIC ACID (UNII: PQ6CK8PD0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83872-519-01 260 g in 1 BOX, UNIT-DOSE; Type 0: Not a Combination Product 11/11/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 11/11/2024 Labeler - Shenzhen Xiaomai Manufacturing Co., Ltd. (712999147) Establishment Name Address ID/FEI Business Operations Shenzhen Xiaomai Manufacturing Co., Ltd. 712999147 manufacture(83872-519)