Label: BANSBAO SKIN BRIGHTENING AND SPOTS-REMOVING- salicylic acid cream
-
Contains inactivated NDC Code(s)
NDC Code(s): 72889-526-95 - Packager: Mengfei Li Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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.
Drug Label Information
Updated April 4, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
- Purpose
- Uses
-
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, use only one topical acne medication at a time, Avoid contact with eyes. If contact occurs, flush thoroughly with water.
- Direction. Cleanse twice a day
- Other Information:
-
Inactive ingredients:
Water, glycerin, propylene glycol, squalane, dimethicone, cyclomethicone, hydroxyethyl urea, glycine, ammonium polyacryloyldimethyl taurate, tocopherol, glucose, mannose, polyglucuronic acid, sodium hyaluronate, Prunus persica (peach) flower extract, Nelumbo nucifera flower extract, Hibiscus militaris flower extract, methylparaben, caprylhydroxamic acid, glyceryl caprylate, disodium EDTA, fragrance.
- SPL UNCLASSIFIED SECTION
- Packaging
-
INGREDIENTS AND APPEARANCE
BANSBAO SKIN BRIGHTENING AND SPOTS-REMOVING
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72889-526 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 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SQUALANE (UNII: GW89575KF9) DIMETHICONE (UNII: 92RU3N3Y1O) CYCLOMETHICONE (UNII: NMQ347994Z) HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR) GLYCINE (UNII: TE7660XO1C) AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (55000 MPA.S) (UNII: F01RIY4371) TOCOPHEROL (UNII: R0ZB2556P8) ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK) MANNOSE, L- (UNII: 2W3YE50TX8) POLYGALACTURONIC ACID (UNII: VV3XD4CL04) HYALURONATE SODIUM (UNII: YSE9PPT4TH) PRUNUS PERSICA FLOWER (UNII: 19GWB0JENH) NELUMBO NUCIFERA FLOWER (UNII: 61W322NLDV) HIBISCUS LAEVIS FLOWER (UNII: 10813RME15) METHYLPARABEN (UNII: A2I8C7HI9T) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) FAGRAEA BERTEROANA FLOWER OIL (UNII: 6665W245VP) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72889-526-95 1 in 1 BOX 01/20/2019 1 50 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 final part333D 01/20/2019 Labeler - Mengfei Li Inc. (116958347)
