Dr. Guard Pack Solid

Manufacturer
JBK FORMS Co Ltd
Effective date
2021-11-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:44:49

Label at a glance#

ProductDr. Guard Pack Solid
Active ingredientSODIUM CHLORITE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

sodium chlorite

INACTIVE INGREDIENT SECTION

citric acid, water

OTC - PURPOSE SECTION

Disinfectant · Deodorizer

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

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 SECTION

■ For external use only.

■ Do not use in eyes.

■ lf swallowed, get medical help promptly.

■ Stop use, ask doctor lf irritation occurs.

■ Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82358-0005-12023-01-30C16284748780-1f386c64a-281f-0266-e053-dadaa90a7c1aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82358-0005-1Dr. Guard Pack Solid3 g in 1 CONTAINERPOWDER31

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82358-0005DR. GUARD PACK SOLID (SODIUM CHLORITE) POWDER [JBK FORMS CO LTD]1Legacy NDC, 1 package rows20211109_d03fe7a8-a280-6e8a-e053-2a95a90a9d00.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82358-000582358-0005-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM CHLORITEG538EBV4VFACTIB
CITRIC ACID MONOHYDRATE2968PHW8QPIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d03fe746-baad-6f37-e053-2995a90a2479d03fe7a8-a280-6e8a-e053-2a95a90a9d002021-11-07WarningsExact identifier
spl id: d03fe746-baad-6f37-e053-2995a90a2479
spl set id: d03fe7a8-a280-6e8a-e053-2a95a90a9d00

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.