Label: SUPER WHITE STUFF PAIN RELIEF- menthol cream
- NDC Code(s): 14448-445-00
- Packager: BLUE SPRING WELLNESS
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 23, 2024
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- 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 clear up and occur again within few days.
- Directions:
-
Inactive Ingredients:
Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Anthemis Nobilis (Roman Chamomile) Oil, Aqua (Deionized Water), Argania Spinosa (Argan) Oil, Arnica Montana Flower Extract, Ascorbyl Palmitate (Vitamin C), Calendula Officinalis Extract, Caprylyl Glycol, Centaurea Cyanus (Cornflower) Extract, Chamomilla Recutita (Chamomile) Extract, Coriandrum Sativum (Coriander) Oil, Emu Oil, Glycerin, Hamamelis Virginiana (Witch Hazel), Lamium Album (White Nettle) Extract, Methylsulfonylmethane (MSM), Phenoxyethanol, Salix Nigra (Willow) Bark Extract, Sodium Cocoyl Isethionate, Sodium Hydroxide, Sorbitol, Tanacetum Parthenium (Feverfew) Extract, Tetrasodium EDTA, Tilia Cordata (Linden) Extract, Tocopheryl Acetate (Vitamin E), Vitis Vinifera (Grape) Seed Extract.
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
SUPER WHITE STUFF PAIN RELIEF
menthol creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:14448-445 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 ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) ARGAN OIL (UNII: 4V59G5UW9X) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) ASCORBYL PALMITATE (UNII: QN83US2B0N) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CHAMOMILE (UNII: FGL3685T2X) CORIANDER (UNII: 1OV56052IK) EMU OIL (UNII: 344821WD61) GLYCERIN (UNII: PDC6A3C0OX) WITCH HAZEL (UNII: 101I4J0U34) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) PHENOXYETHANOL (UNII: HIE492ZZ3T) SALIX NIGRA BARK (UNII: QU52J3A5B3) SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493) SODIUM HYDROXIDE (UNII: 55X04QC32I) SORBITOL (UNII: 506T60A25R) FEVERFEW (UNII: Z64FK7P217) 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:14448-445-00 118 mL in 1 JAR; Type 0: Not a Combination Product 03/04/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 03/04/2024 Labeler - BLUE SPRING WELLNESS (182950118)