Label: STAIN REMOVER (stain remover- bamboo liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 82371-003-01 - Packager: Zhejiang Dibao Biotechnology Co., Ltd.
- 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.
Drug Label Information
Updated December 28, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- HOW TO USE
- INDICATIONS & USAGE
- KEEP OUT OF REACH OF CHILDREN
- PURPOSE
- STORAGE AND HANDLING
-
WARNINGS
1.Do not directly expose the processed stain area to sunlight.
2.Keep out of reach of children.
3. If got into eyes, please rinse with plenty of water immediately. Ask doctor for help if necessary.
4. If swallowed, please go to the hospital immediately and show the doctor product container and label. - PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
STAIN REMOVER
stain remover(bamboo) liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82371-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOXYNOL-11 (UNII: SQL994V0M6) (OCTOXYNOL-11 - UNII:SQL994V0M6) OCTOXYNOL-11 4 g in 100 mL BAMBUSA VULGARIS TOP (UNII: FIW80T6P6V) (BAMBUSA VULGARIS TOP - UNII:FIW80T6P6V) BAMBUSA VULGARIS TOP 10.2 g in 100 mL SODIUM LAURYL SULFATE (UNII: 368GB5141J) (LAURYL SULFATE - UNII:DIQ16UC154) SODIUM LAURYL SULFATE 8 g in 100 mL C12-15 PARETH-10 (UNII: Z0QJT9586T) (C12-15 PARETH-10 - UNII:Z0QJT9586T) C12-15 PARETH-10 5 g in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: 94255I6E2T) BETAINE (UNII: 3SCV180C9W) WATER (UNII: 059QF0KO0R) COCO DIETHANOLAMIDE (UNII: 92005F972D) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82371-003-01 8.9 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/28/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/28/2021 Labeler - Zhejiang Dibao Biotechnology Co., Ltd. (603023294) Establishment Name Address ID/FEI Business Operations Zhejiang Dibao Biotechnology Co., Ltd. 603023294 manufacture(82371-003)