Active Ingredients
Menthol 0.5%
Lavaderm Aftersun Spray
FDA Label NDC 70631-067
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Young Living Essential Oils, Lc. for the product Lavaderm Aftersun (NDC 70631-067). 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, uses:, warnings:, when using this product, stop use and ask a doctor if, keep out of reach of children to avoid accidental ingestion., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Topical Analgesic
Uses:
For the temporary relief of pain and itching associated with: minor burns, sunburn, minor cuts, scrapes, insect bites, minor skin irritations.
Warnings:
For external use only
When Using This Product
avoid contact wiith eyes
Stop Use And Ask A Doctor If
- condition worsens
- symptoms last more than 7 days or clear up and occur again within a few days
Keep Out Of Reach Of Children To Avoid Accidental Ingestion.
If swallowed, get medical help or contact Poison Control Center right away.
Directions
Shake well. Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: Ask a doctor.
Inactive Ingredients
water, olive oil, glycerin, safflower oil, sunflower oil, jojoba oil, polyglyceryl-10 pentastearate, glyceryl monocaprylate, helianthus annuus seed wax, european elderberry, xanthan gum, docosanol, sodium stearoyl lactylate, lavender oil, aloe vera leaf, glyceryl monoundecylenate, phytate sodium, picea mariana leaf oil, helichrysum italicum flower oil, citric acid
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