LA VAQUITA NEW EXTRA- methyl salicylate, menthol ointment

La Vaquita by

Drug Labeling and Warnings

La Vaquita by is a Otc medication manufactured, distributed, or labeled by Delon Laboratories (1990) Ltd, Laboratoires Delon. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

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
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 not final	part348	04/26/2011

Labeler - Delon Laboratories (1990) Ltd (248364184)

Establishment
Name	Address	ID/FEI	Business Operations
Delon Laboratories (1990) Ltd		243387722	label(61734-301) , manufacture(61734-301) , pack(61734-301)