Label: SUPER WHITE STUFF PAIN RELIEF- menthol cream
- NDC Code(s): 14448-306-40
- Packager: BLUE SPRING WELLNESS, L.L.C.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 10, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- 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 occur again within a few days.
- Other information
- Directions
-
Inactive Ingrediets
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 Extract.
- Questions or Comments?
- Package Labeling:130ml
-
INGREDIENTS AND APPEARANCE
SUPER WHITE STUFF PAIN RELIEF
menthol creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:14448-306 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) WATER (UNII: 059QF0KO0R) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) ASCORBYL PALMITATE (UNII: QN83US2B0N) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CHAMOMILE (UNII: FGL3685T2X) TANACETUM PARTHENIUM WHOLE (UNII: 6GE7Z0761K) CORIANDER (UNII: 1OV56052IK) 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:14448-306-40 130 mL in 1 JAR; Type 0: Not a Combination Product 08/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 08/01/2020 Labeler - BLUE SPRING WELLNESS, L.L.C. (182950118)