S PANAX ALL IN ONE MIST- sodium benzoate liquid 
S AND PANAX CO LTD

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.

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Sodium benzoate

Dendropanax morbiferus Extract

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

■ 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.

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

for topical use only

label

S PANAX ALL IN ONE MIST 
sodium benzoate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81885-0002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM BENZOATE (UNII: OJ245FE5EU) (BENZOIC ACID - UNII:8SKN0B0MIM) SODIUM BENZOATE0.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81885-0002-180 mL in 1 BOTTLE; Type 0: Not a Combination Product05/18/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/18/2021
Labeler - S AND PANAX CO LTD (695447279)
Registrant - S AND PANAX CO LTD (695447279)
Establishment
NameAddressID/FEIBusiness Operations
S AND PANAX CO LTD695447279manufacture(81885-0002)

Revised: 2/2023
Document Id: f4a6003e-ea9b-eb37-e053-2995a90abc6a
Set id: c293e8b6-e178-345e-e053-2995a90ad0fd
Version: 2
Effective Time: 20230214
 
S AND PANAX CO LTD