Label: NEROCARE CAPSAICIN NEUROPATHY RELIEF CREAM- capsaicin cream
- NDC Code(s): 84066-108-01
- Packager: Guangzhou Tata Biotechnology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 3, 2026
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
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INACTIVE INGREDIENT
INACTIVE INGREDIENTS:
GLYCERIN, WATER, MINERAL OIL, BUTYROSPERMUM PARKII (SHEA) BUTTER, DIMETHICONE, CETEARYL ALCOHOL, GLYCERYL STEARATE, PHENOXYETHANOL, PEG-100 STEARATE, POLYACRYLAMIDE, METHYLPARABEN, C13-14 ISOPARAFIN, MENTHYL LACTATE, BHT, ALLANTOIN, DIMETHICONOL, LAURETH-7, FRAGRANCE, DISODIUM EDTA, XANTHAN GUM, BUTYLENE GLYCOL, ARNICA MONTANA FLOWER EXTRACT, 1,2-HEXANEDIOL, HYDROXYACETOPHENONE
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DOSAGE & ADMINISTRATION
Directions:
1.Clean and dry skin.
2.Apply an appropriate amount evenly toaffected areas such as your back,neck,knees,hips,shoulders and elbows,3.Massage gently until absorbed.
4.Allow the area to dry naturally after application
5.Apply a small amount of the product tothe affected area 2-3 times daily.
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OTHER SAFETY INFORMATION
Storage:
1.Please seal the product and store it in acool,dry place away from direct sunlight,
2.Do not store it in damp or high,temperatureenvironments like bathrooms,kitchens,or refrigerators.
3.Keep it out of children's reach,lftheproduct changes in characteristics(eg:oil separation or abnormal odor)discontinue use.
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
NEROCARE CAPSAICIN NEUROPATHY RELIEF CREAM
capsaicin creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84066-108 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM) CAPSAICIN 0.1 g in 100 g Inactive Ingredients Ingredient Name Strength PHENOXYETHANOL (UNII: HIE492ZZ3T) METHYLPARABEN (UNII: A2I8C7HI9T) ALLANTOIN (UNII: 344S277G0Z) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) MINERAL OIL (UNII: T5L8T28FGP) DIMETHICONE (UNII: 92RU3N3Y1O) MENTHYL LACTATE (UNII: 2BF9E65L7I) WATER (UNII: 059QF0KO0R) GLYCERYL STEARATE (UNII: 230OU9XXE4) LAURETH-7 (UNII: Z95S6G8201) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) BHT (UNII: 1P9D0Z171K) CETEARYL ALCOHOL (UNII: 2DMT128M1S) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) XANTHAN GUM (UNII: TTV12P4NEE) BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y) PEG-100 STEARATE (UNII: YD01N1999R) DIMETHICONOL (40 CST) (UNII: 343C7U75XW) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84066-108-01 100 g in 1 TUBE; Type 0: Not a Combination Product 04/03/2026 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 04/03/2026 Labeler - Guangzhou Tata Biotechnology Co., Ltd. (699605102)
