Label: CHLORINE DIOXIDE AIR DISINFECTANT powder
-
Contains inactivated NDC Code(s)
NDC Code(s): 55090-001-01 - Packager: Chengdu Xinyi Kaiwei Medical Equipment Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
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 May 6, 2020
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
- ACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
- PURPOSE
-
WARNINGS
1. External disinfectant should not be taken orally;Keep out of reach of children;
2. Should not be mixed with other disinfectants, alkali or organic matter;
3. This product can bleach,It shall not be used for disinfection of metal articles;
4. Avoid contact with skin and inhalation of high concentration disinfectant;
5. The product should be kept away from fire and heat source;
6. Do not use in wet places such as rain, high temperature and places with long time sun exposure;
7. Do not breathe near the nose or directly;
8. If the. disinfectant accidentally touches. the eyes,rinse with water immediately, or seek medical advice in severe cases. - PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
CHLORINE DIOXIDE AIR DISINFECTANT
chlorine dioxide air disinfectant powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55090-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORINE DIOXIDE (UNII: 8061YMS4RM) (CHLORINE DIOXIDE - UNII:8061YMS4RM) CHLORINE DIOXIDE 130 mg in 6.5 g Inactive Ingredients Ingredient Name Strength CALCIUM CHLORIDE (UNII: M4I0D6VV5M) SODIUM BISULFATE (UNII: BU8V88OWIQ) SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) SODIUM CHLORITE (UNII: G538EBV4VF) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55090-001-01 6.5 g in 1 BOTTLE; Type 0: Not a Combination Product 05/06/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/06/2020 Labeler - Chengdu Xinyi Kaiwei Medical Equipment Co., Ltd. (550900665) Establishment Name Address ID/FEI Business Operations Chengdu Xinyi Kaiwei Medical Equipment Co., Ltd. 550900665 manufacture(55090-001)