- Drug Facts
- Active ingredients
- Purpose
- Uses
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Warnings
For external use only
Do not use
•on wounds •irritated or damaged skin •sensitive skin
•with a heating pad •if pregnant
•with, or as the same time as, other external analgesic products
•if allergic to aspirin or salicylates
•if allergic to any ingredients of this product
When using this product
•avoid contact with the eyes •do not bandage tightly
•do not apply to wounds or damaged skin
•do not use 1 hour before or after bathing
Stop use and ask a doctor if
•condition worsens •symptoms persist for more than 7 days
•symptoms clear up and occur again within a few days
•excessive irritation of the skin develops
•redness is present •side effects occur.
If pregnant, ask a health professional before use.
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other Information
- Inactive Ingredients
- Question or Comments?
- SPL UNCLASSIFIED SECTION
- Packaging
-
INGREDIENTS AND APPEARANCE
PAIN RELIEF HERBAL BALM
methyl salicylate, menthol, camphor ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68233-807 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 207.3 mg in 1 g MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM 155.5 mg in 1 g CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL) 31.1 mg in 1 g Inactive Ingredients Ingredient Name Strength EUCALYPTUS OIL (UNII: 2R04ONI662) LAVENDER OIL (UNII: ZBP1YXW0H8) PETROLATUM (UNII: 4T6H12BN9U) WHITE WAX (UNII: 7G1J5DA97F) Product Characteristics Color yellow Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68233-807-01 1 in 1 BOX 09/01/2006 1 50 g in 1 JAR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 09/01/2006 Labeler - Albert Max, Inc. (149445798)