Label: (QIQING) SODIUM HYPOCHLORITE DISINFECTANT- sodium hypochlorite liquid
Contains inactivated NDC Code(s)
NDC Code(s): 77919-003-01, 77919-003-02, 77919-003-03, 77919-003-04
- Packager: Qingdao precision medical technology co., LTD. Zibo branch
- 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.
Updated June 21, 2020
If you are a consumer or patient please visit this version.
- Active Ingredient(s)
This product is a topical disinfectant and cannot be mixed with other disinfection products.
It’s recommended to wear gloves and avoid contact with the skin during use. If the original solution comes in contact with the skin, rinse it with water; if it gets in eyes, immediately rinse it with water.
Don’t dilute with hot water above 40 ℃.
Corrosive to metals and bleaching to fabrics.
It’s normal to have a few floating objects and sediments, and you can continue to use them.
Store in a closed, dark, cool and dry place. Use it as soon as possible after opening.
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
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
- Other information
- Inactive ingredients
Package Label - Principal Display Panel
Qiqing® Sodium Hypochlorite disinfectant
MAIN ACTIVE INGREDIENT AND CONTENT
The main active ingredient is sodium hypochlorite, the effective chlorine content is 4% ~ 6%(w/v).
Kills intestinal pathogens, pyogenic cocci, common bacteria and bacterial spores from hospital infections.
INGREDIENTS AND APPEARANCE
(QIQING) SODIUM HYPOCHLORITE DISINFECTANT
sodium hypochlorite liquid
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77919-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM HYPOCHLORITE (UNII: DY38VHM5OD) (HYPOCHLORITE ION - UNII:T5UM7HB19N) SODIUM HYPOCHLORITE 6 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77919-003-01 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/21/2020 2 NDC:77919-003-02 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/21/2020 3 NDC:77919-003-03 5000 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/21/2020 4 NDC:77919-003-04 10000 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/21/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/21/2020 Labeler - Qingdao precision medical technology co., LTD. Zibo branch (554534589) Registrant - Qingdao precision medical technology co., LTD. Zibo branch (554534589) Establishment Name Address ID/FEI Business Operations Qingdao precision medical technology co., LTD. Zibo branch 554534589 manufacture(77919-003)