Label: DISINFECTANT LIQUID ANTIBACTERIAL- disinfectant liquid antibacterial spray spray
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Contains inactivated NDC Code(s)
NDC Code(s): 74534-014-01, 74534-014-02, 74534-014-03, 74534-014-04, view more74534-014-05, 74534-014-06, 74534-014-07, 74534-014-08, 74534-014-09, 74534-014-10, 74534-014-11, 74534-014-12 - Packager: Guangzhou Dedo Pharmaceutical 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 April 24, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
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Directions
GENERAL OBJECT AND SKIN DISINFECTION:DIRECT SPRAYING OF PRODUCTS ON GENERAL OBJECTS OR SKIN SURFACES REQUIRING DISINFECTION;FRUITS AND VEGETABLES DISINFECTION:SPRAY DIRECTLY ON THE FRUIT AND VEGETABLE SURFACE AND FINSE WITH WATER AFTER 10 MINUTES
Children under 6 years of age should be supervised when using this product.
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
DISINFECTANT LIQUID ANTIBACTERIAL
disinfectant liquid antibacterial spray sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74534-014 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID 0.02 g in 100 g Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74534-014-01 500 g in 1 BOTTLE; Type 0: Not a Combination Product 04/13/2020 2 NDC:74534-014-12 600 g in 1 BOTTLE; Type 0: Not a Combination Product 04/13/2020 3 NDC:74534-014-02 300 g in 1 BOTTLE; Type 0: Not a Combination Product 04/13/2020 4 NDC:74534-014-03 200 g in 1 BOTTLE; Type 0: Not a Combination Product 04/13/2020 5 NDC:74534-014-04 100 g in 1 BOTTLE; Type 0: Not a Combination Product 04/13/2020 6 NDC:74534-014-05 120 g in 1 BOTTLE; Type 0: Not a Combination Product 04/13/2020 7 NDC:74534-014-07 1000000 g in 1 BOTTLE; Type 0: Not a Combination Product 04/13/2020 8 NDC:74534-014-06 250 g in 1 BOTTLE; Type 0: Not a Combination Product 04/13/2020 9 NDC:74534-014-08 100000 g in 1 BOTTLE; Type 0: Not a Combination Product 04/13/2020 10 NDC:74534-014-09 50000 g in 1 BOTTLE; Type 0: Not a Combination Product 04/13/2020 11 NDC:74534-014-10 2000 g in 1 BOTTLE; Type 0: Not a Combination Product 04/13/2020 12 NDC:74534-014-11 1000 g in 1 BOTTLE; Type 0: Not a Combination Product 04/13/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/13/2020 Labeler - Guangzhou Dedo Pharmaceutical Co.,Ltd (418394705) Registrant - Guangzhou Dedo Pharmaceutical Co.,Ltd (418394705) Establishment Name Address ID/FEI Business Operations Guangzhou Dedo Pharmaceutical Co.,Ltd 418394705 manufacture(74534-014)