Country: Bandaríkin
Tungumál: enska
Heimild: NLM (National Library of Medicine)
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ), MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)
Delon Laboratories (1990) Ltd
METHYL SALICYLATE
METHYL SALICYLATE 12 g in 100 g
TOPICAL
OTC DRUG
Topical analgesic - for the temporary relief of minor aches and pains of muscles and joints
OTC monograph not final
LA VAQUITA NEW EXTRA- METHYL SALICYLATE, MENTHOL OINTMENT DELON LABORATORIES (1990) LTD ---------- LA VAQUITA EXTRA _ACTIVE INGREDIENTS_ Menthol 3% Methyl Salicylate 12% _PURPOSE_ Topical analgesic _USES_ for the temporary relief of minor aches and pains of muscles and joints _WARNINGS_ FOR EXTERNAL USE ONLY WHEN USING THIS PRODUCT avoid contact with the eyes do not bandage tightly do not apply to wounds or damaged skin STOP USE AND ASK A DOCTOR IF condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days IF PREGNANT OR BREAST-FEEDING, ask a health professional before use. 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 older: apply to affected area not more than 3 to 4 times daily children under 2 years of age: consult a doctor _INACTIVE INGREDIENTS_ D&C red no. 17, lanolin, paraffin, petrolatum LA VAQUITA NEW EXTRA methyl salicylate, menthol ointment PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:61734-301 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 12 g in 100 g MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 3 g in 100 g INACTIVE INGREDIENTS Delon Laboratories (1990) Ltd INGREDIENT NAME STRENGTH PETROLATUM (UNII: 4T6H12BN9U) PARAFFIN (UNII: I9O0E3H2ZE) LANOLIN (UNII: 7EV65EAW6H) D&C RED NO. 17 (UNII: ND733RX3JN) PACKAGING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:61734-301- 01 90 g in 1 CAN; Type 0: Not a Combination Product 10/04/2014 2 NDC:61734-301- 02 100 g in 1 JAR; Type 0: Not a Combination Product 07/18/2018 MARKETING INFORMATION MARKETING CATEGORY APPLICATION NUMBER OR MONOGRAPH CITATION MARKETING START DATE MARKETING END DATE OTC Monograph Drug M017 04/26/2011 LABELER - Delon Laboratories (1990) Ltd (248364184) ESTABLISHME Lestu allt skjalið