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Drug Facts
The following Structured Product Label (SPL) was submitted to the FDA by Strategic Sourcing Services, Llc for the product Camphor Spirit (NDC 70677-1201). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding other, active ingredient, purpose, indication, warnings, when using this product, discontinue use and consult a doctor if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Camphor 10%
External Anagesic
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 apply to wounds or irritated skin.
Avoid getting in the eyes.
If swallowed, immediately give 3 or 4 glasses 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.
Do not bandage tightly.
condition worsens, or if excesive irritation develops.
symptoms persit for more than 7 days, or clear up and occur again within a few days.
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.
Adults and children 2 yrs. and older. apply to the affected area not more than 3 or 4 times daily.
Children under 2 yrs of age: Do not use, consult a doctor.
Flammable: Keep away from spark, heat and flame.
Alcohol 84%, Purified Water
* Please review the disclaimer below.