Label: DETERGENT FOR CARS (detergent for cars- bamboo liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 82371-002-01 - 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 30, 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
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DIRECTIONS
This product can not be on the surface of silicone products for a long time.This product can not be used on leather surface.
Spray enough product where you need to clean up to cover the dirt.
Children should be supervised when using this product.
When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask doctor if irritation or rash appears and lasts. 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
- PURPOSE
- STORAGE AND HANDLING
- WARNINGS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DETERGENT FOR CARS
detergent for cars(bamboo) liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82371-002 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 3.2 g in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM METABISULFITE (UNII: 4VON5FNS3C) SODIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: 94255I6E2T) TRIMETHYL OCTADECYL AMMONIUM CHLORIDE (UNII: CZ70647U92) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82371-002-01 473 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(82371-002)