Label: PAIN RELIEVING CREAM- camphor and menthol cream
- NDC Code(s): 84338-001-09
- Packager: PAIN WIZARD LIMITED LIABILITY COMPANY
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 6, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
- Purpose
- Uses
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Warnings
For external use only
When using this product
- use only as directed
- avoid contact with the eyes and mucous membranes
- do not apply to wounds or damaged, broken or irritated skin
- do not bandage tightly or apply local heat (such as heating pads) to the area of use
- Directions
- Other information
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Inactive ingredients
Aloe Barbadensis Leaf Juice, Ananas Sativus (Pineapple) Fruit Extract, Arnica Montana Flower Extract, Benzoic Acid, Boswellia Carterii Resin Extract, Camellia Sinensis Flower Extract, Capsicum Annuum Extract, Carbomer, Decyl Glucoside, Glycerin, Hamamelis Virginiana (Witch Hazel) Water, Methyl Sulfonyl Methane, Phenoxyethanol, Propylene Glycol, Rosa Centifolia Flower Extract, Salix Alba (Willow) Bark Extract, Sodium Hydroxide, Sorbic Acid, Vitis Vinifera (Grape) Seed Extract, Water, Zingiber Officinale (Ginger) Root Extract
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INGREDIENTS AND APPEARANCE
PAIN RELIEVING CREAM
camphor and menthol creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84338-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 3 mg in 100 mL MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 3 mg in 100 mL Inactive Ingredients Ingredient Name Strength BENZOIC ACID (UNII: 8SKN0B0MIM) VITIS VINIFERA SEED (UNII: C34U15ICXA) SALIX ALBA BARK (UNII: 205MXS71H7) ALOE VERA LEAF (UNII: ZY81Z83H0X) ROSA CENTIFOLIA FLOWER (UNII: CS4TE8FF7O) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) CAPSICUM (UNII: 00UK7646FG) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) SORBIC ACID (UNII: X045WJ989B) GINGER (UNII: C5529G5JPQ) SODIUM HYDROXIDE (UNII: 55X04QC32I) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) FRANKINCENSE (UNII: R9XLF1R1WM) PHENOXYETHANOL (UNII: HIE492ZZ3T) WATER (UNII: 059QF0KO0R) CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17) ANANAS SATIVUS (PINEAPPLE) FRUIT (UNII: 2A88ZO081O) HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V) GLYCERIN (UNII: PDC6A3C0OX) CARBOMER COPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 1N11AG4X4L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84338-001-09 88.7 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 12/02/2004 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 12/02/2004 Labeler - PAIN WIZARD LIMITED LIABILITY COMPANY (802945597)