SUNMARK CAMPHOR SPIRIT- camphor 10% liquid 
Strategic Sourcing Services LLC

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Sunmark Camphor Spirit USP


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

Questions or Comments?

1-800-662-3435

Principal Display Panel

Camphor Spirits, USP

label

SUNMARK CAMPHOR SPIRIT 
camphor 10% liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49348-148
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)100 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49348-148-3059 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/12/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01701/01/2008
Labeler - Strategic Sourcing Services LLC (116956644)
Registrant - Pharma Nobis, LLC (118564114)
Establishment
NameAddressID/FEIBusiness Operations
Pharma Nobis, LLC118564114manufacture(49348-148) , analysis(49348-148) , pack(49348-148) , label(49348-148)

Revised: 12/2023
Document Id: 0ce56aeb-f940-fa74-e063-6294a90aa548
Set id: 667b3a9f-4a5c-4ef0-adbd-cce9a5f94faa
Version: 6
Effective Time: 20231219
 
Strategic Sourcing Services LLC