Label: LBRI STOP THE PAIN SUPER ALOE PAIN RELIEF CREAM- menthol, methyl salicylate cream
- NDC Code(s): 71238-492-00, 71238-492-01
- Packager: L'BRI HEALTH AND BEAUTY INC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 5, 2023
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- DRUG FACTS:
- Active Ingredients
- Uses:
-
Warnings:
For external use only.
Stop use and ask a doctor if
rash or irritation develops and lasts. condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.
- Directions:
- Other Information:
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Inactive ingredients:
a-Bisabolol, Allantoin, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Flower Extract, Calendula Officinalis Extract, Caprylic/Capric Triglyceride, Capsaicin, Carbomer, Cetearyl Alcohol, Ceteareth-20, Ethylhexylglycerin, Eucalyptus Globulus Oil, Euterpe Oleracea (Acai Berry) Fruit Extract, Glucosamine sulfate, Glycerin, Glyceryl Stearate, Magnesium Sulfate, Malus Domestica (Apple) Fruit Cell Culture Extract, Mentha Piperita (Peppermint) Oil, Methylsulfonylmethane (MSM), PEG-100 Stearate, Phenoxyethanol, Polysorbate-20, Rosmarinus Officinalis (Rosemary) Extract, Stearic Acid, Symphytum Offiinale (Comfrey) Extract, Tocopheryl Acetate (Vitamin E), Triethanolamine, ZIngiber Officinalis (Ginger) Extract.
- Package Labeling:
- Package Labeling:
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INGREDIENTS AND APPEARANCE
LBRI STOP THE PAIN SUPER ALOE PAIN RELIEF CREAM
menthol, methyl salicylate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71238-492 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 50 mg in 1 mL METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 100 mg in 1 mL Inactive Ingredients Ingredient Name Strength MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB) APPLE (UNII: B423VGH5S9) PEPPERMINT OIL (UNII: AV092KU4JH) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) PEG-100 STEARATE (UNII: YD01N1999R) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYSORBATE 20 (UNII: 7T1F30V5YH) ROSEMARY (UNII: IJ67X351P9) STEARIC ACID (UNII: 4ELV7Z65AP) SYMPHYTUM X UPLANDICUM LEAF (UNII: D05HXK6R3G) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TROLAMINE (UNII: 9O3K93S3TK) GINGER (UNII: C5529G5JPQ) ALLANTOIN (UNII: 344S277G0Z) ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CAPSAICIN (UNII: S07O44R1ZM) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) EUCALYPTUS OIL (UNII: 2R04ONI662) ACAI (UNII: 46AM2VJ0AW) GLUCOSAMINE SULFATE (UNII: 1FW7WLR731) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71238-492-00 118 mL in 1 TUBE; Type 0: Not a Combination Product 06/19/2023 2 NDC:71238-492-01 5 mL in 1 PACKET; Type 0: Not a Combination Product 06/19/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M015 06/19/2023 Labeler - L'BRI HEALTH AND BEAUTY INC (139751148)