SunX SPF 30/BugX Wallmount
SunX SPF 30/BugX Wallmount is an FDA drug label for the active ingredient SUNX SPF 30/BUGX WALLMOUNT manufactured by CoreTex Products Inc. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231022.
- Generic name
- SUNX SPF 30/BUGX WALLMOUNT
- Manufacturer
- CoreTex Products Inc
- Product type
- HUMAN OTC DRUG
- Route
- N/A
- Dosage form
- N/A
- NDC
- 65753-511
- Application
- N/A
- Label effective
- 20231022
About this product
SunX SPF 30/BugX Wallmount is an FDA-registered drug product whose active ingredient is SUNX SPF 30/BUGX WALLMOUNT. It is labelled by CoreTex Products Inc and marketed as a human otc drug product. Identifiers on file: NDC 65753-511, label effective 20231022. It is one of 2 FDA drug label records sharing the active ingredient SUNX SPF 30/BUGX WALLMOUNT. 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.
What it is used for
Across FDA labelling, products containing SUNX SPF 30/BUGX WALLMOUNT are most often described in connection with: helps prevent, sunburn higher, spf gives, protetion retains, minutes activity, water sweating, provides high, protection against. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses helps prevent sunburn higher SPF gives more sunburn protetion. retains SPF after 80 minutes of activity in the water or sweating provides high protection against sunburn.
Dosage & Administration
Directions apply liberally 15 minutes before sun exposure Reapply: after 80 minutes of swimming or sweating after towel drying, swimming , or at least every 2 hours children under 6 months of age: Ask a doctor
Warnings
Warnings For external use only. Do not use on damaged or broken skin When using this product keep out of the eyes. Rinse with water to remove. Stop use and ask a doctor if rash or irritation develops and lasts Keep out of the reach of children If swallowed get medical help or contact a Poison Control center right away.
How products containing SUNX SPF 30/BUGX WALLMOUNT compare
FDA lists 2 drug label records with SUNX SPF 30/BUGX WALLMOUNT 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.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | CoreTex Products Inc | 2 |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
Frequently asked questions
What is SunX SPF 30/BugX Wallmount used for?
Uses helps prevent sunburn higher SPF gives more sunburn protetion. retains SPF after 80 minutes of activity in the water or sweating provides high protection against sunburn.
Who makes SunX SPF 30/BugX Wallmount?
CoreTex Products Inc is the labeler of record for SunX SPF 30/BugX Wallmount. 2 FDA label records share the active ingredient SUNX SPF 30/BUGX WALLMOUNT, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.
Is SunX SPF 30/BugX Wallmount 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 SUNX SPF 30/BUGX WALLMOUNT?
Yes. 2 FDA drug label records list SUNX SPF 30/BUGX WALLMOUNT 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 SunX SPF 30/BugX Wallmount 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.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.