S PANAX ALL IN ONE LIQUIDSOAP- salt liquid

s panax all in one liquidsoap by

Drug Labeling and Warnings

s panax all in one liquidsoap 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

july

INACTIVE INGREDIENT

Dendropanax morbiferus Extract, salt, Lauric acid, Stearic acid, Olive oil, Natural Betain, Ricinus Communis(Castir) Seed Oil, Glycerin, Sodium hyaluronate, Lavenda oil, pepper mint oil, Tea Tree Oil, Naoh , Coconut oil

PURPOSE

1. NO Corona virus
2. Sterilization, antibacterial, deodorant, fragrance, multi-functional mist
3. World Atopy Association verification completed
4. Excellent moisture retention with patented natural hwangchil extract
5. 100% Hwangchil extract (natural ingredient)
6. It is not sticky and does not dry after sprinkling.

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 LIQUIDSOAP 
salt liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81885-0001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SEA SALT (UNII: 87GE52P74G) (SEA SALT - UNII:87GE52P74G)	SEA SALT	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
LAURIC ACID (UNII: 1160N9NU9U)
GLYCERIN (UNII: PDC6A3C0OX)
STEARIC ACID (UNII: 4ELV7Z65AP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81885-0001-1	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/18/2021
2	NDC: 81885-0001-2	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(81885-0001)