Label: SUPER WHITE STUFF PAIN RELIEF- menthol cream
- NDC Code(s): 14448-315-00
- Packager: BLUE SPRING WELLNESS, L.L.C.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 10, 2023
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- Official Label (Printer Friendly)
- Active Ingredient:
- Uses:
-
Warnings:
For external use only.
Stop use and ask a doctor if
you experience a rash and/or a reaction, condition worsens, or if symptoms persist for more than 10 days or clears up and occurs again within a few days.
- Directions:
- Other Information:
-
Inactive Ingredients:
Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Anthemis Nobilis (Roman Chamomile) Oil, Aqua (Deionized Water), Arnica Montana Flower Extract, Ascorbyl Palmitate (Vitamin C), Calendula Officinalis Extract, Caprylyl Glycol, Centraurea Cyanus (Cornflower) Extract, Chamomilla Recutita (Chamomile) Extract, Chrysanthemum Parthenium (Feverfew) Extract, Coriandrum Sativum (Coriander) Oil, Emu Oil, Hamamelis Virginiana (Witch Hazel), Lamium Album (White Nettle) Extract, Methylsulfonylmethane (MSM), Phenoxyethanol, Salix Nigra (Willow) Bark Extract, Sodium Cocoyl Isethionate, Sodium Hydroxide, Sorbitol, Tetrasodium EDTA, Tilia Cordata (Linden) Extract, Tocopheryl Acetate (Vitamin E), Vitis Vinifera (Grape) Seed Extarct.
- Package Labeling:
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INGREDIENTS AND APPEARANCE
SUPER WHITE STUFF PAIN RELIEF
menthol creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:14448-315 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 14 mg in 1 mL Inactive Ingredients Ingredient Name Strength CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) ALOE VERA LEAF (UNII: ZY81Z83H0X) CHAMAEMELUM NOBILE FLOWER OIL (UNII: UB27587839) WATER (UNII: 059QF0KO0R) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) ASCORBYL PALMITATE (UNII: QN83US2B0N) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CENTAUREA CYANUS FLOWER (UNII: QZ239038YC) CHAMOMILE (UNII: FGL3685T2X) TANACETUM PARTHENIUM WHOLE (UNII: 6GE7Z0761K) CORIANDER OIL (UNII: 7626GC95E5) EMU OIL (UNII: 344821WD61) HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) LAMIUM ALBUM WHOLE (UNII: 046Y1357I6) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) PHENOXYETHANOL (UNII: HIE492ZZ3T) SALIX NIGRA BARK (UNII: QU52J3A5B3) SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493) SODIUM HYDROXIDE (UNII: 55X04QC32I) SORBITOL (UNII: 506T60A25R) EDETATE SODIUM (UNII: MP1J8420LU) TILIA CORDATA WHOLE (UNII: W5E5UB44GD) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) VITIS VINIFERA SEED (UNII: C34U15ICXA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:14448-315-00 5 mL in 1 PACKET; Type 0: Not a Combination Product 04/19/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 04/19/2021 Labeler - BLUE SPRING WELLNESS, L.L.C. (182950118)