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

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.


HUMCO Camphor Spirit

Drug Facts

Active Ingredient

Camphor 10%




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


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.


(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?


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camphor spirit.jpg

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
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
#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 not finalpart34801/01/2008
Labeler - Humco Holding Group, Inc. (825672884)
NameAddressID/FEIBusiness Operations
Humco Holding Group, Inc.825672884manufacture(0395-0467) , analysis(0395-0467) , pack(0395-0467) , label(0395-0467)

Revised: 2/2020
Document Id: 9e2fff93-65c2-61ea-e053-2a95a90a5da4
Set id: 9a0ef0a3-3c79-41b2-8193-424a3ef9886f
Version: 3
Effective Time: 20200209
Humco Holding Group, Inc.