MENTHOLATUM- methyl salicylate, dl-menthol lotion

País: Estados Unidos

Língua: inglês

Origem: NLM (National Library of Medicine)

Ingredientes ativos:

METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ), MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)

Disponível em:

Lydia Co., Ltd.

Via de administração:

TOPICAL

Tipo de prescrição:

OTC DRUG

Indicações terapêuticas:

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

Status de autorização:

unapproved drug other

Características técnicas

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