Ülke: ABD
Dil: İngilizce
Kaynak: NLM (National Library of Medicine)
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ), MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)
Lydia Co., Ltd.
TOPICAL
OTC DRUG
temporary relief aches and pains of muscles and joints associated with: • arthritis • simple backache • sprains • strains • bruises ■ Adults and children 2 years of age and older: apply to the affected area no more than 3 to 4 times daily ■ children under 2 years of age: consult a doctor
unapproved drug other
MENTHOLATUM- METHYL SALICYLATE, DL-MENTHOL LOTION LYDIA 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._ ---------- Methyl Salicylate, DL-Menthol temporary relief aches and pains of muscles and joints associated with: • arthritis • simple backache • sprains • strains • bruises Keep out of reach of children ■ Adults and children 2 years of age and older: apply to the affected area no more than 3 to 4 times daily ■ children under 2 years of age: consult a doctor Warnings For external use only. Flammable ■ Keep away from fire, flame, sparks and heated surfaces. Tight cap firmly. Stop use and ask a doctor if ■ Condition worsens or symptoms persist for more than 7days or clear up and occur again within a few days When using this product ■ Use only as direct ■ Avoid contact with eyes ■ Do not apply to wounds or damaged skin ■ Do not bandage tightly If pregnant or breast-feeding, ask a health professional before use Keep out of reach of childre mineral oil, lantrol, Sorbitan Monostearate, etc topocal use MENTHOLATUM Lydia Co., Ltd. methyl salicylate, dl-menthol lotion PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:72988-0031 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ 4LPZ ) METHYL SALICYLATE 200 mg in 1 g MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 60 mg in 1 g INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH MINERAL OIL (UNII: T5L8T28FGP) WATER (UNII: 059QF0KO0R) PACKAGING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:72988- 0031-1 75 g in 1 BOTTLE; Type 0: Not a Combination Product 09/30/2022 MARKETING INFORMATION MARKETING CATEGORY APPLICATION NUMBER OR MONOGRAPH CITATION MARKETING START DATE MARKETING END DATE unapproved drug other 09/30/2022 LA Belgenin tamamını okuyun