BEEVENOM- methyl salicylate ointment

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients:

Methyl Salicylate 10.5%

PURPOSE

External analgesic

Uses

For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains and sprains.

Warnings

For external use only

Do not use

• On wounds or damaged skin
• with a heating pad
• on a child under 12 years of age
• over extensive areas of the body
• on irritated skin
• with a bandage

ASK DOCTOR

Ask A doctor use if you have:

• redness over the affected area

When using this product, do not

• avoid contact with eyes or mucous membranes
• do not bandage

Stop use and ask a doctor if:

• condition worsens or symptoms persist for more than 7 days
• symptoms clear up and occur again within a few days
• excessive skin irritation occurs

If pregnant or breastfeeding

ask a health professional before use

Keep Out Of reach of children

If swallowed, induce vomiting and call a physician or contact Poison Control Center right away.

Directions:

• use only as directed
• Adults and children 2 years and older: apply to affected area not more than 3 to 4 time daily
• children under 12 years of age: ask a doctor

Other Information

Store at 15ºC to 25 o C (59ºF to 77ºF)

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Inactive ingredients:

Camphor, D&C yellow #10, menthol, methylparaben, paraffin wax, propylparaben, white petrolatum

Beevenom Ointment

INGREDIENTS AND APPEARANCE

BEEVENOM 
methyl salicylate ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53145-315
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	10.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PETROLATUM (UNII: 4T6H12BN9U)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
MENTHOL (UNII: L7T10EIP3A)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
PARAFFIN (UNII: I9O0E3H2ZE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53145-315-05	150 g in 1 JAR; Type 0: Not a Combination Product	04/01/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	04/01/2026

Labeler - Menper Distributors, Inc. (101947166)

Establishment
Name	Address	ID/FEI	Business Operations
DRLZ Enterprises		031125329	manufacture(53145-315)