CAMPHOR SPIRIT- camphor 10% liquid

Camphor Spirit by

Drug Labeling and Warnings

Camphor Spirit by is a Otc medication manufactured, distributed, or labeled by Pharma Nobis, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Camphor 10%

Purpose

Counterirritant

Use

For the temporary relief of minor aches, muscle and joint pain associated with arthritis, strains, brusies and simple backache.

Warnings

For external use only.

Do not drink. If swallowed, immediately give 3 or 4 glases of water. Do not induce vomiting. If vomiting occurs, give fluids again. Do not give anything by mouth to an unconscious or convulsing person. Get medical attention immediately.

Avoid contact with eyes or mucous membranes.

Do not apply to irritated skin.

When using this product

Do not bandage tightly.

Discontinue use and consult a doctor if

condition worsens, or if excesive irritation develops.

symptoms persit for more than 7 days, or clear up and occur again within a few days.

Keep out of reach of children

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center right away. In case of eye contact, flush eyes with running water for 15 minutes, get medical attention.

Directions

(dilute 3 parts olive oil and mix well)

Adults and children 2 yrs. and older. apply to th affected area not more than 3 or 4 times daily.

Children under 2 yrs of age: consult a doctor befre use.

Other Information

Flammable: Keep away from spark, heat and flame.

Inactive ingredients

Alcohol 84%, Purified Water

Sunmark Label

Leader Label

Quality Choice Label

DDM Label

INGREDIENTS AND APPEARANCE

CAMPHOR SPIRIT 
camphor 10% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82645-920
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941)	CAMPHOR (NATURAL)	100 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82645-920-92	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/12/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	01/01/2008

Labeler - Pharma Nobis, LLC (118564114)

Registrant - Pharma Nobis, LLC (118564114)

Establishment
Name	Address	ID/FEI	Business Operations
Pharma Nobis, LLC		118564114	manufacture(82645-920) , analysis(82645-920) , pack(82645-920) , label(82645-920)