DR. GUARD PACK SOLID- sodium chlorite powder

Dr. Guard Pack Solid by

Drug Labeling and Warnings

Dr. Guard Pack Solid by is a Otc medication manufactured, distributed, or labeled by JBK FORMS Co Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

sodium chlorite

INACTIVE INGREDIENT

citric acid, water

PURPOSE

Disinfectant · Deodorizer

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF THE CHILDREN

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

■ 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

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR. GUARD PACK SOLID 
sodium chlorite powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82358-0005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6)	SODIUM CHLORITE	10 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82358-0005-1	3 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(82358-0005)