Label: REAL TIME PAIN RELIEF MAXX PLUS TOPICAL ANALGESIC- menthol lotion
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NDC Code(s):
84573-547-03,
84573-547-04,
84573-547-05,
84573-547-07, view more84573-547-12, 84573-547-16
- Packager: Real Time Products Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 12, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Uses:
-
Warnings:
For external use only
When using this product:
Use only as directed
- Avoid contact with eyes or mucous membranes
- Do not apply to wounds or damaged skin
- Do not bandage tightly
- Directions:
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Other Ingredients:
*Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Flower Extract, Calendula Officinalis Extract, Cannabis Sativa (Hemp)Seed Oil, Caprylyl Glycol, Capsaicin, Centaurea Cyanus (Cornflower) Extract, Chamomilla Matricaria (Chamomile) Extract, Chondroitin Sulfate, Coriandrum Sativum (Coriander) Fruit Oil, Emu Oil, Glucosamine Sulfate, Glycerin, Hamamelis Virginiana (Witch Hazel), Hypericum Perforatum (St. John's Wort) Extract, C13-14 Isoparaffin, Laureth-7, Mentha Piperita (Peppermint) Oil, Methylsulfonylmethane (MSM), Phenoxyethanol, Polyacrylamide, Salix Alba (Willow) Bark Extract, SD-Alcohol 40B, Sorbitol, Tilia Cordata (Linden) Bark Extract. *Denotes certified organic ingredient.
- Questions?
- Package Labelling: 88ml
- Package Labelling: 120ml
- Package Labelling: 147.8ml
- Package Labelling: 210ml
- Package Labelling: 354ml
- Package Labelling: 473ml
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INGREDIENTS AND APPEARANCE
REAL TIME PAIN RELIEF MAXX PLUS TOPICAL ANALGESIC
menthol lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84573-547 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 19 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) HEMP (UNII: TD1MUT01Q7) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CAPSAICIN (UNII: S07O44R1ZM) CHAMOMILE (UNII: FGL3685T2X) CORIANDER OIL (UNII: 7626GC95E5) EMU OIL (UNII: 344821WD61) GLUCOSAMINE SULFATE (UNII: 1FW7WLR731) GLYCERIN (UNII: PDC6A3C0OX) WITCH HAZEL (UNII: 101I4J0U34) ST. JOHN'S WORT (UNII: UFH8805FKA) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) LAURETH-7 (UNII: Z95S6G8201) PEPPERMINT OIL (UNII: AV092KU4JH) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) PHENOXYETHANOL (UNII: HIE492ZZ3T) SALIX ALBA (WILLOW) BARK EXTRACT (UNII: 205MXS71H7) SORBITOL (UNII: 506T60A25R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84573-547-03 88 mL in 1 TUBE; Type 0: Not a Combination Product 10/23/2024 2 NDC:84573-547-04 120 mL in 1 TUBE; Type 0: Not a Combination Product 10/23/2024 3 NDC:84573-547-05 147.8 mL in 1 TUBE; Type 0: Not a Combination Product 10/23/2024 4 NDC:84573-547-07 210 mL in 1 TUBE; Type 0: Not a Combination Product 10/23/2024 5 NDC:84573-547-12 354 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/23/2024 6 NDC:84573-547-16 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/23/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 10/23/2024 Labeler - Real Time Products Inc. (117624292)