Label: REAL TIME PAIN RELIEF FOOT- menthol cream
- NDC Code(s): 84573-515-04, 84573-515-06, 84573-515-08
- Packager: Real Time Products Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 24, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Uses:
-
Warnings:
Do notapply to wounds or damaged skin or bandage tightly.
For external use only.
Stop use and ask doctor if:
Condition worsens
- Symptoms persist for more than 7 days or clear up and occur again within a few days.
- Directions:
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Inactive Ingredients
Allantoin, *Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Anthemis Nobilis (Roamn Chamomile) Oil, Aqua (Deionized Water), Ascorbic Acid (Vitamin-C), Calendula Officinalis Extract, Caprylyl Glycol, Centaurea Cyanus (Cornflower) Extract, Ceresin Wax, Cetearyl Alcohol, Cetyl Alcohol, Chamomilla Mantricaria (Chamomile) Extract, Coriandrum Sativum (Coriander) Oil, Emu Oil, Eucalyptus Globulus Oil, Glycerin, Hydrogenated Vegetable Oil, Hypericum Perforatum (St.John's Wort), Lactic Acid, Lanolin, Melaleuca Alternifolia (Tea Tree) Oil, Petrolatum, Phenoxyethanol, Polysorbate-20, Polysorbate-80, Retinyl Palmitate (Vitamin A), Salix Alba (Willow) Bark Extract, SD-Alcohol 40B, Sodium Borate, SorbitanSesquioleate, Stearyl Alcohol, Tilia Cordata (Linden) Bark Extract, Tocopheryl Acetate (Vitamin E).
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- Package Labelling:
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INGREDIENTS AND APPEARANCE
REAL TIME PAIN RELIEF FOOT
menthol creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84573-515 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 15 mg in 1 g Inactive Ingredients Ingredient Name Strength ALLANTOIN (UNII: 344S277G0Z) ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) ASCORBIC ACID (UNII: PQ6CK8PD0R) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CERESIN (UNII: Q1LS2UJO3A) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETYL ALCOHOL (UNII: 936JST6JCN) CHAMOMILE (UNII: FGL3685T2X) CORIANDER (UNII: 1OV56052IK) EMU OIL (UNII: 344821WD61) EUCALYPTUS OIL (UNII: 2R04ONI662) GLYCERIN (UNII: PDC6A3C0OX) ST. JOHN'S WORT (UNII: UFH8805FKA) LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT) LANOLIN (UNII: 7EV65EAW6H) MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K) PETROLATUM (UNII: 4T6H12BN9U) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYSORBATE 20 (UNII: 7T1F30V5YH) POLYSORBATE 80 (UNII: 6OZP39ZG8H) VITAMIN A (UNII: 81G40H8B0T) SALIX ALBA BARK (UNII: 205MXS71H7) SODIUM BORATE (UNII: 91MBZ8H3QO) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84573-515-04 125 g in 1 JAR; Type 0: Not a Combination Product 07/12/2024 2 NDC:84573-515-06 170 g in 1 JAR; Type 0: Not a Combination Product 07/12/2024 3 NDC:84573-515-08 226 g in 1 JAR; Type 0: Not a Combination Product 07/12/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 07/12/2024 Labeler - Real Time Products Inc. (117624292)



