Active Ingredients Purpose
Camphor – 0.5% External Analgesic
The following Structured Product Label (SPL) was submitted to the FDA by Biological Health Group Corporation for the product Formula A (NDC 69711-006). 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 active ingredients purpose, purpose, uses, warnings, otc - pregnancy or breast feeding, stop use and ask a doctor if, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Camphor – 0.5% External Analgesic
External analgesic
• For the temporary relief of pain and itching associated with minor skin irritations.
For external use only.
Avoid contact with eyes.
If you are breastfeeding, consult a health care practitioner prior to use.
• if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again, discontinue use of this product and consult a doctor .
Keep out of reach of the children. If overdose or accidental ingestion occurs, call a Poison Control Center immediately.
Apply to affected areas not more than 1-3 times daily.
Water, Glycerin, Arnica Oil, Eucalyptus Essential Oil, Apricot Kernel Oil, Essential Oils of Tea Tree and Rosemary,Vitamin A and E, Grapefruit Seed Extract.
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Do not use if you are allergic to plants of the Asteraceae/Compositae/Daisy family. Hypersensitivity, such as allergy, has been known to occur; in which case, discontinue use.
Consult a health care practitioner if symptoms persist or worsen.
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