SANAR NATURALS ARNICA PAIN RELEIVING ROLL ON WITH CAMPHOR- camphor liquid

Sanar Naturals Arnica Pain Releiving Roll On with Camphor by

Drug Labeling and Warnings

Sanar Naturals Arnica Pain Releiving Roll On with Camphor by is a Otc medication manufactured, distributed, or labeled by Sanvall Enterprises, Inc, Evi Labs. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Camphor 1%

Purpose

Pain Relief

Uses

For the temporary relief of minor aches and pains of muscles joints

Warnings

For external use only

Avoid contact with eyes.

Do not

use on wounds or damaged skin

bandage tightly

Stop use and ask a doctor if

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

Keep out of reach of children.

is swallowed, get medical help or contact Poison Control Center right away

Directions

• Adults and children over 12 years: Apply to affected area no more than 3 to 4 times daily.
• Children under 12 years: Do not use, consult a doctor.

Other Information

Store tightly closed in a dry place at controlled room temperature between 59-77 F (15-25 C)

Inactive ingredients

Aqua, Arnica Montana Flowe Extract, Propylene Glycol, Menthol, Glycerin, Carbomer, Methyl Salicylate, Ththanolamine, Eucalyptus Globulus Leaf Oil, Disodium EDTA, Tocopheryl Acetate, Capsicum Annum Fruit Extract, Methylchloroisothiazolinone, Methylisothiazolinone.

Label copy

INGREDIENTS AND APPEARANCE

SANAR NATURALS ARNICA PAIN RELEIVING ROLL ON WITH CAMPHOR 
camphor liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73386-148
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	1 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
METHYL SALICYLATE (UNII: LAV5U5022Y)
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
CAPSICUM FRUTESCENS WHOLE (UNII: 6XJX33L87P)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
WATER (UNII: 059QF0KO0R)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
MENTHOL (UNII: L7T10EIP3A)
CARBOMER 980 (UNII: 4Q93RCW27E)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73386-148-03	88.5 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	01/01/2024

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

Labeler - Sanvall Enterprises, Inc (966905507)

Establishment
Name	Address	ID/FEI	Business Operations
Evi Labs		123617598	manufacture(73386-148)