S PANAX ALL IN ONE MIST- sodium benzoate liquid

s panax all in one mist by

Drug Labeling and Warnings

s panax all in one mist by is a Otc medication manufactured, distributed, or labeled by S AND PANAX CO LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Sodium benzoate

INACTIVE INGREDIENT

Dendropanax morbiferus Extract

PURPOSE

Corona virus, Sterilization, antibacterial, deodorant, fragrance, multi-functional liquid soap

WARNINGS

■ if following abnormal symptoms persist, discontinue use

Irritation around the eyes, ears, mucous membranes, including the mouth, under the skin irritation and rashes

■ Stop immediately and consult a doctor if you experience

1) Hypersensitivity symptoms such as erythema, itching and dermatitis.

2) Skin Irritation

3) Following Instructions when using medication

(1) For external use only (Do not use internally)

(2) Avoid getting into the eyes (if contact occurs, wash well with clean water)

■ Be careful not to inhale or use excessively for a long time (ingesting ethanol repeatedly causes irritation to mucous membranes and headaches or other symptoms may appear. When used repeatedly in the same area, skin irritation may occur.

■ Do not use the product for a long time in the same area as swelling, inflammation or sickness may occur due to absorption through the skin.

It is not recommended to use this one areas that have been medically treated with a cast or bandage.

■ Do not use in combination with soap or antibacterial cleansing agents.

KEEP OUT OF REACH OF CHILDREN

Keep Out of Reach of Children.

INDICATIONS & USAGE

■ Pour a small amount into hands, spread evenly and rub into the skin

DOSAGE & ADMINISTRATION

for topical use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

S PANAX ALL IN ONE MIST 
sodium benzoate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81885-0002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM BENZOATE (UNII: OJ245FE5EU) (BENZOIC ACID - UNII:8SKN0B0MIM)	SODIUM BENZOATE	0.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81885-0002-1	80 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/18/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/18/2021

Labeler - S AND PANAX CO LTD (695447279)

Registrant - S AND PANAX CO LTD (695447279)

Establishment
Name	Address	ID/FEI	Business Operations
S AND PANAX CO LTD		695447279	manufacture(81885-0002)