Ülke: ABD
Dil: İngilizce
Kaynak: NLM (National Library of Medicine)
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A), METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)
Kinray Inc.
MENTHOL
MENTHOL .076 g in 100 g
TOPICAL
OTC DRUG
Uses Temporarily relieves minor pain associated with: arthritis, simple backache, muscle strains, bruises, sprains and cramps. Purpose Pain relieving gel.
OTC monograph not final
PAIN RELIEF BALMPREFERRED PLUS PH PREFERRED PLUS PHARMACY- MENTHOL GEL KINRAY INC. _Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they_ _comply with applicable regulations and policies. FDA has not evaluated whether this product complies._ ---------- DRUG FACTS Menthol 7.6% Methyl Salicylate 29.0% USES Temporarily relieves minor pain associated with: arthritis, simple backache, muscle strains, bruises, sprains and cramps. WARNINGS FOR EXTERNAL USE ONLY. ALLERGY ALERT: IF PRONE TO ALLERGIC REACTION FROM ASPIRIN OR SALICYLATES, CONSULT A DOCTOR BEFORE USE. WHEN USING THIS PRODUCT: USE ONLY AS DIRECTED, AVOID CONTACT WITH THE EYES OR MUCUS MEMBRANES, DO NOT BANDAGE TIGHTLY OR USE WITH A HEATING PAD, DO NOT APPLY TO WOUNDS OR DAMAGED SKIN. STOP USE AND ASK DOCTOR IF: CONDITION GETS WORSE, SYMPTOMS LAST MORE THAN 7 DAYS, OR SYMPTOMS CLEAR UP AND OCCUR AGAIN IN A FEW DAYS. IF PREGNANT OR BREAST-FEEDING: ASK A HEALTHCARE PROFESSIONAL BEFORE USE. DIRECTIONS Adults and children 12 years of age and older: apply generously to affected area. Massage into painful are until thoroughly absorbed into skin. Repeat as necessary, but not more than 4 times daily. Children under 12 years of age: ask doctor. INACTIVE INGREDIENTS Paraffin, White Petrolatum. PURPOS E Pain relieving gel. KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center right away. PREFERRED PLUS PHARMACY COOL 'N HEAT THERAPY PAIN RELIEF BALM Kinray Inc. PAIN RELIEF BALMPREFERRED PLUS PH PREFERRED PLUS PHARMACY menthol gel PRODUCT INFORMATION PRODUCT T YPE HUMAN OTC DRUG ITE M CODE (SOURCE ) NDC:6 1715-0 20 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRE NG TH MENTHO L (UNII: L7T10 EIP3A) (MENTHOL - UNII:L7T10 EIP3A) MENTHOL .0 76 g in 10 0 g METHYL SALICYLATE (UNII: LAV5U50 22Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE .29 g in 10 0 g INACTIVE INGREDIENTS INGREDIENT NAME STRE NG TH PARAFFIN (UNII: I9 O0 E3H2 Belgenin tamamını okuyun