DR. SANA ALIVIO TOTAL ALIVIO TOTAL ROLL ON- alivio total roll on cream

DR. SANA ALIVIO TOTAL by

Drug Labeling and Warnings

DR. SANA ALIVIO TOTAL by is a Otc medication manufactured, distributed, or labeled by EVI LABS. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Camphor 3 %

Menthol 1.25 %

Purpose

Camphor 3%.......Topical Analgesic Cream

Menthol 1.25 %....Topical Analgesic Cream

Uses

Temporarily relieves minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises and sprains.

Warnings

For external use only. Avoid contact with the eyes.

Flammable: Keep away from excessive heat or open flame.

Do not use

• On wounds or damaged skin
• With a heating pad
• On a child under 2 years of age with this product

When using this product

• Avoid contact with eyes or mucous membranes
• Do not bandage tightly
• Do not apply to irritated skin

Stop use and ask a doctor if

Condition worsens
Symptoms persist for more than 7 days
Symptoms clear up and occur again within a few days

Excessive skin irritation occurs

Keep out of reach of children

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

Directions

Adults and children 2 years and older: apply to affected areas not more than 3 to 4 times daily. Children under 2 years: ask a doctor

Other information

Store at 20–25°C (68–77°F). Protect from excessive heat

Inactive Ingredients

Water (Aqua), Methyl Salicylate, Glycerin, Cetearyl Alcohol, Mineral Oil (Paraffinum Liquidum), Glyceryl Stearate, Eucalyptus Globulus Leaf Oil, Polysorbate 20, Phenoxyethanol, Xanthan Gum, Disodium EDTA, Tocopheryl Acetate, Arnica Montana Flower Extract, Triethanolamine.

Questions or comments

Call weekdays from 9.30 am to 5 pm EST at Tel. 305-633-7900

Label principal panel display panel

INGREDIENTS AND APPEARANCE

DR. SANA ALIVIO TOTAL  ALIVIO TOTAL ROLL ON
alivio total roll on cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84178-108
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	1.106 g  in 88.5 g
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	2.655 g  in 88.5 g

Inactive Ingredients
Ingredient Name	Strength
ARNICA MONTANA (UNII: O80TY208ZW)	0.025 g  in 88.5 g
WATER (UNII: 059QF0KO0R)	65.643 g  in 88.5 g
GLYCERIN (UNII: PDC6A3C0OX)	2.655 g  in 88.5 g
CETEARYL ALCOHOL (UNII: 2DMT128M1S)	2.655 g  in 88.5 g
XANTHAN GUM (UNII: TTV12P4NEE)	0.2665 g  in 88.5 g
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)	0.044 g  in 88.5 g
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)	0.885 g  in 88.5 g
PHENOXYETHANOL (UNII: HIE492ZZ3T)	0.885 g  in 88.5 g
EDETATE DISODIUM (UNII: 7FLD91C86K)	0.177 g  in 88.5 g
EUCALYPTOL (UNII: RV6J6604TK)	0.885 g  in 88.5 g
POLYSORBATE 20 (UNII: 7T1F30V5YH)	0.885 g  in 88.5 g
GAULTHERIA PROCUMBENS (WINTERGREEN) LEAF OIL (UNII: LAV5U5022Y)	7.965 g  in 88.5 g
MINERAL OIL (UNII: T5L8T28FGP)	1.77 g  in 88.5 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84178-108-01	88.5 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/22/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	03/22/2026

Labeler - EVI LABS (123617598)

Establishment
Name	Address	ID/FEI	Business Operations
EVI LABS		123617598	manufacture(84178-108)