Label: DR. GUARD SPECIAL CAR EDITION REFILL STICK- sodium chlorite liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 82358-0004-1 - Packager: JBK FORMS 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 4, 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
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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INDICATIONS & USAGE
How to Use (How to Activate)
- The stick contains a main liquid solution and an ampoule inside that includes active
ingredients in powder form.
Bend the middle part of the stick to break the ampoule.
Once the ampoule inside the stick cracks, sufficiently shake the stick to mix the powder
with the solution well.
As it turns yellow, the stick is activated and the pure chlorine dioxide is released through
the surface of the stick.
After 3~4 weeks of usage, the stick will turn transparent which indicates that it is no
longer effective. Please dispose the used stick into a general trash bag. - WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DR. GUARD SPECIAL CAR EDITION REFILL STICK
sodium chlorite liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82358-0004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6) SODIUM CHLORITE 5 g in 100 g Inactive Ingredients Ingredient Name Strength CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82358-0004-1 4 g in 1 CONTAINER; Type 0: Not a Combination Product 11/04/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 11/04/2021 Labeler - JBK FORMS Co Ltd (695637869) Registrant - JBK FORMS Co Ltd (695637869) Establishment Name Address ID/FEI Business Operations JBK FORMS Co Ltd 695637869 manufacture(82358-0004)
