SATOHAP- methyl salicylate, dl-camphor, l-menthol lotion 
Sato Pharmaceutical Co., Ltd.

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Satohap Lotion

Active ingredients
dl-Camphor 5%
l-Menthol 4%
Methyl salicylate 10%

Purpose
dl-Camphor    External analgesic
l-Menthol    External analgesic
Methyl salicylate    External analgesic

Uses

temporarily relieves minor aches and pains of muscles and joints due to
■ backache     ■ arthritis     ■ strains     ■ bruises     ■ sprains

Warnings
For external use only

Do not use

■ on wounds

■ on damaged or irritated skin


When using this product

■ avoid contact with the eyes and mucous membranes

■ do not bandage tightly

Stop use and ask a doctor if

■ excessive irritation develops

■ condition worsens

■ symptoms persist for more than 7 days

■ symptoms clear up and occur again within a few days

■ when using for pain of arthritis if:

■ pain persist for more than 10 days

■ redness is present

■ in conditions affecting children under 12 years of age


Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions
■ adults and children 2 years of age and over: apply to affected area not more than 3 to 4 times daily.
■ children under 2 years of age: do not use, ask a doctor.

Inactive ingredients
edetate disodium, alcohol, propylene glycol, water

Satohap Lotion Carton

SATOHAP 
methyl salicylate, dl-camphor, l-menthol lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49873-065
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE10 g  in 100 mL
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)5 g  in 100 mL
LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7) LEVOMENTHOL4 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
EDETATE DISODIUM (UNII: 7FLD91C86K)  
ALCOHOL (UNII: 3K9958V90M)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49873-065-011 in 1 CARTON02/05/1991
145 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01702/05/1991
Labeler - Sato Pharmaceutical Co., Ltd. (690575642)
Establishment
NameAddressID/FEIBusiness Operations
Sato Pharmaceutical Co., Ltd.715699133manufacture(49873-065) , label(49873-065) , pack(49873-065)

Revised: 12/2023
Document Id: 0b7d6dc4-82df-04b0-e063-6394a90af9ec
Set id: 348fde05-2797-4410-a1b2-99e64187c4fe
Version: 4
Effective Time: 20231201
 
Sato Pharmaceutical Co., Ltd.