Peep Club
Peep Club is an FDA drug label for the active ingredient GLYCERIN manufactured by Peep Club Eyecare Corp. administered by OPHTHALMIC. 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 20260528.
- Generic name
- GLYCERIN
- Manufacturer
- Peep Club Eyecare Corp.
- Product type
- HUMAN OTC DRUG
- Route
- OPHTHALMIC
- Dosage form
- N/A
- NDC
- 87581-100
- Application
- M018
- Label effective
- 20260528
About this product
Peep Club is an FDA-registered drug product whose active ingredient is GLYCERIN. It is labelled by Peep Club Eyecare Corp. taken by ophthalmic and marketed as a human otc drug product. Identifiers on file: NDC 87581-100, application M018, label effective 20260528. It is one of 37 FDA drug label records sharing the active ingredient GLYCERIN. 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 GLYCERIN are most often described in connection with: lubricant prevent, irritation relieve. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses For use as a lubricant to prevent further irritation or to relieve dryness of the eye.
Dosage & Administration
Directions for application to closed eyelids only close both eyes apply 1-2 sprays on each eyelid by fully pressing the nozzle from a distance of 6-10 inches use as needed replace cap after use
Warnings
Warnings For external use only. Do not use if solution changes color or becomes cloudy When using this product do not touch tip of container to any surface to avoid contamination. Replace cap after using use within 6 months of opening or by expiration date safe to use with contact lenses Stop use and ask a doctor if you experience eye pain, changes in vision, continued redness or irritation of the eye condition worsens or lasts for more than 72 hours Keep out of reach of children. If swallowed get medical help or contact a Poison control center right away.
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View labelHow products containing GLYCERIN compare
FDA lists 37 drug label records with GLYCERIN 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 |
|---|---|---|---|
| — | — | Shantou Ximonth Biotechnology Co., Ltd. | 12 |
| — | — | Guangzhou Houkea Biotechnology Co., Ltd. | 4 |
| — | — | Shantou Eelhoe Daily Chemical Technology Co., Ltd. | 4 |
| — | — | Shantou Ouhoe Technology Co., Ltd. | 3 |
| — | — | Beijing Jingfeng Pharmaceutical (Shandong) Co., Ltd | 2 |
Frequently asked questions
What is Peep Club used for?
Uses For use as a lubricant to prevent further irritation or to relieve dryness of the eye.
Who makes Peep Club?
Peep Club Eyecare Corp. is the labeler of record for Peep Club. 37 FDA label records share the active ingredient GLYCERIN, 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 Peep Club come in?
administered by ophthalmic. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Peep Club 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 GLYCERIN?
Yes. 37 FDA drug label records list GLYCERIN 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 Peep Club 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.