HUMCO CAMPHOR SPIRIT- camphor 10% liquid 
Humco Holding Group, Inc.

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HUMCO Camphor Spirit


Drug Facts

Active Ingredient

Camphor 10%

Purpose

External analgesic

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.

Do not use undiluted product.

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 before 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 Spiritscamphor spirit.jpg

HUMCO CAMPHOR SPIRIT 
camphor 10% liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0395-0467
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:0395-0467-16473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2013
2NDC:0395-0467-9259 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2013
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01701/01/2008
Labeler - Humco Holding Group, Inc. (825672884)
Registrant - Pharma Nobis, LLC (118564114)
Establishment
NameAddressID/FEIBusiness Operations
Pharma Nobis, LLC118564114manufacture(0395-0467) , analysis(0395-0467) , pack(0395-0467) , label(0395-0467)

Revised: 12/2023
Document Id: 0c92eeea-202f-e81a-e063-6394a90a48eb
Set id: 9a0ef0a3-3c79-41b2-8193-424a3ef9886f
Version: 6
Effective Time: 20231215
 
Humco Holding Group, Inc.