NERVEX PAIN RELIEVING- capsaicin cream

Nervex Pain Relieving by

Drug Labeling and Warnings

Nervex Pain Relieving by is a Otc medication manufactured, distributed, or labeled by VITA SCIENCES, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Capsaicin 0.03%

Purpose

Topical Analgesic

Uses:

• For temporary relief of minor aches and pains.

Warnings:

For external use only

Do not

• apply to wounds or damaged skin. 
• bandage tightly.

When using this product

• Avoid contact with the eyes.

Stop use and ask a doctor if

• condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

If pregnant or breast-feeding,

ask a health professional before use

Directions:

• Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.
• Children under 2 years of age: consult a doctor.

Other information:

• Protect the product in this container from excessive heat and direct sun.

Inactive ingredients:

Andrographis Paniculata Extract, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Amica Montana Flower Extract, Behentrimonium Methosulfate, Caprylic/Capric Triglyceride, Cetearyl Alcohol, Cetereath-20, Cetyl Alcohol, Cetyl Myristoleate, Cholecalciferol (Vitamin D3), dl-Panthenol, Emulsifying Wax NF, Glycerin, Hamamelis Virginiana (Witch Hazel) Distillate, Helianthus Annuus (Sunflower) Oil, Methylcobalamin (Vitamin B12), Methylsulfonylmethane (MSM), Phenoxyethanol, Potassium Sorbate, Pyridoxine (Vitamin B6), Sodium Bicarbonate, Stearic Acid, Thiamine (Vitamin B1), Tocopherol (Vitamin E).

Questions?

(877) 212-7282

Package Labelling:

INGREDIENTS AND APPEARANCE

NERVEX PAIN RELIEVING 
capsaicin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84834-542
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM)	CAPSAICIN	0.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ANDROGRAPHIS PANICULATA WHOLE (UNII: 0P49L952WZ)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
CETYL ALCOHOL (UNII: 936JST6JCN)
CETYL MYRISTOLEATE (UNII: 87P8K33Q5X)
CHOLECALCIFEROL (UNII: 1C6V77QF41)
PANTHENOL (UNII: WV9CM0O67Z)
GLYCERIN (UNII: PDC6A3C0OX)
WITCH HAZEL (UNII: 101I4J0U34)
HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
CYANOCOBALAMIN (UNII: P6YC3EG204)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
PYRIDOXINE (UNII: KV2JZ1BI6Z)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
STEARIC ACID (UNII: 4ELV7Z65AP)
THIAMINE (UNII: X66NSO3N35)
TOCOPHEROL (UNII: R0ZB2556P8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84834-542-00	1 in 1 BOX	10/01/2024
1		50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	10/01/2024

Labeler - VITA SCIENCES, LLC (828327168)