SunBurnt Advanced After-Sun

SunBurnt Advanced After-Sun is an FDA-registered drug product whose active ingredient is CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, CANTHARIS VESICATORIA. It is labelled by Welmedix LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 24330-210, label effective 20180320. It is one of 2 FDA drug label records sharing the active ingredient CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, CANTHARIS VESICATORIA. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Across FDA labelling, products containing CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, CANTHARIS VESICATORIA are most often described in connection with: temporarily relieves, symptoms mild, moderate sunburn, overheated skin, redness rawness, itching dryness, homeopathic materia, drug administration. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses Temporarily relieves symptoms of mild and moderate sunburn such as: overheated skin redness rawness itching dryness Product Uses are based on the Homeopathic Materia Medica. These Uses have not been evaluated by the Food and Drug Administration.

Directions for best results, clean skin and apply immediately to affected area adults and children 2 years of age and older: apply 2-3 times a day, as needed, or as directed by your doctor children under 2 years of age: consult a doctor

Warnings For external use only Do not use on severe sunburn on broken skin if you have a rash if you have an allergy or hypersensitivity to any ingredients When using this product avoid contact with eyes or mucous membranes 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 If pregnant or breast feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

FDA lists 2 drug label records with CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, CANTHARIS VESICATORIA as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is SunBurnt Advanced After-Sun used for?
Uses Temporarily relieves symptoms of mild and moderate sunburn such as: overheated skin redness rawness itching dryness Product Uses are based on the Homeopathic Materia Medica. These Uses have not been evaluated by the Food and Drug Administration.

Who makes SunBurnt Advanced After-Sun?
Welmedix LLC is the labeler of record for SunBurnt Advanced After-Sun. 2 FDA label records share the active ingredient CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, CANTHARIS VESICATORIA, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does SunBurnt Advanced After-Sun come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is SunBurnt Advanced After-Sun prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, CANTHARIS VESICATORIA?
Yes. 2 FDA drug label records list CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, CANTHARIS VESICATORIA as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has SunBurnt Advanced After-Sun been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.