Label: TBOSEN EMERGENCY STERILIZATION CARD- chlorine dioxide sustained release granules granule, delayed release
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Contains inactivated NDC Code(s)
NDC Code(s): 81130-101-01, 81130-101-05 - Packager: Jiangsu Tianbosheng Technology 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 November 23, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Inactive ingredients
- Purpose
- When using
- Do not use
- Stop use
- Ask doctor
- Ask doctor/pharmacist
- KEEP OUT OF REACH OF CHILDREN
- Questions
- Pregnancy or breast feeding
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Indications & usage
Product Features; Gaseous circulation disinfection, 360° without dead corners, fast and effective disinfection, especially suitable for influenza season. The application of the new disinfection technology of A1 grade (the same level as drinking water and salt) recognized by the World Health Organization is non-toxic and has no side effects.
Product Efficacy: Quickly kill bacteria, germs, poisonous bacteria and other microorganisms in the air; Purify formaldehyde, TVOC, smoke poison and other harmful substances in the air; Dispel odor, fishy smell and other peculiar smell.
Usage: Plug-in. Tear open the aluminum foil inner bag, take out the disinfection card, and install the hanging rope or clip; It can be carried with you; It can be trailer or wardrobe; Desks or desks can be placed; It can be used as a space for disinfection, odor removal, antivirus and in addition to formaldehyde.
- Dosage & administration
- Dosage forms & strengths
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Warnings
Precautions:
1. Please do not contact this product directly with skin or close-fitting clothing, please use it on the outermost clothing.
2. Allergic to chlorine dioxide preparation please prohibit the use.
3. It is strictly prohibited to place in drinks or oral sterilization.
4. Please do not place it with food. If you eat it carelessly, please rinse your mouth immediately for medical treatment.
5. Do not use it during sleep.
6. Please put it in an untouchable position for infants, pets and people with cognitive impairment.
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Other Information
1. Storage: Seal. Store in a cool and dry place.
2. Validity Period: It has not been opened for three years, and the validity period after opening is 60 days.
3. If used at intervals, it can be stored in a closed container or bag in a cool and dry place.
4. Due to the release characteristics of the product, taste may be generated during use.
5. The effect will vary according to the usage and place of use. If the air flow is intense and windy, the effect will be affected. - Package label. Principal display panel
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INGREDIENTS AND APPEARANCE
TBOSEN EMERGENCY STERILIZATION CARD
chlorine dioxide sustained release granules granule, delayed releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81130-101 Route of Administration EXTRACORPOREAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORINE DIOXIDE (UNII: 8061YMS4RM) (CHLORINE DIOXIDE - UNII:8061YMS4RM) CHLORINE DIOXIDE 1 g in 10 g Inactive Ingredients Ingredient Name Strength SODIUM MOLYBDATE (UNII: 948QAQ08I1) 0.5 g in 10 g CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) 4 g in 10 g N-ACETYLCAPROLACTAM (UNII: 171CCE77J8) 0.2 g in 10 g SODIUM CHLORIDE (UNII: 451W47IQ8X) 1.75 g in 10 g SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.5 g in 10 g SODIUM CHLORITE (UNII: G538EBV4VF) 2 g in 10 g SODIUM SULFATE (UNII: 0YPR65R21J) 0.04 g in 10 g METHYL BENZOATE (UNII: 6618K1VJ9T) 0.01 g in 10 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81130-101-05 5 in 1 BOX 11/23/2020 1 NDC:81130-101-01 10 g in 1 DOSE PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 11/23/2020 Labeler - Jiangsu Tianbosheng Technology Co., Ltd. (412583651) Registrant - Jiangsu Tianbosheng Technology Co., Ltd. (412583651) Establishment Name Address ID/FEI Business Operations Jiangsu Tianbosheng Technology Co., Ltd. 412583651 label(81130-101) , manufacture(81130-101)
