SHREK WAFFLE AND SSYRUP HAND SANITIZING WIPES
SHREK WAFFLE AND SSYRUP HAND SANITIZING WIPES is an FDA drug label for the active ingredient HAND SANITIZING WIPES manufactured by Zhejiang Bright Care Co., Ltd administered by TOPICAL. 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 20260601.
- Generic name
- HAND SANITIZING WIPES
- Manufacturer
- Zhejiang Bright Care Co., Ltd
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 85844-522
- Application
- M003
- Label effective
- 20260601
About this product
SHREK WAFFLE AND SSYRUP HAND SANITIZING WIPES is an FDA-registered drug product whose active ingredient is HAND SANITIZING WIPES. It is labelled by Zhejiang Bright Care Co., Ltd taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85844-522, application M003, label effective 20260601. It is one of 16 FDA drug label records sharing the active ingredient HAND SANITIZING WIPES. 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 HAND SANITIZING WIPES are most often described in connection with: decrease bacteria, skin recommended. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
To decrease bacteria on the skin Recommended for repeated use
Dosage & Administration
Wipe hands, skin surface thoroughly; Allow to dry. Use as needed for skin disinfection. For external use only.
Warnings
For external use only. When using this product key away from eye In case of eye contact, rinse eyes with doctor. Stop use and ask a doctor if: irritation and redness develop. If condition persists for more than 72 hours consult a doctor. Keep out of reach of children. If swallowed, get medical help or contact Poison Control Centre right away
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View labelHow products containing HAND SANITIZING WIPES compare
FDA lists 16 drug label records with HAND SANITIZING WIPES 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 |
|---|---|---|---|
| — | — | Zhejiang Bright Care Co., Ltd | 14 |
| — | — | Innovative Biodefense | 1 |
| — | — | KING KEY MBC LIFE TECHNOLOGY GROUP CO., LTD | 1 |
| — | — | — | — |
| — | — | — | — |
Frequently asked questions
What is SHREK WAFFLE AND SSYRUP HAND SANITIZING WIPES used for?
To decrease bacteria on the skin Recommended for repeated use
Who makes SHREK WAFFLE AND SSYRUP HAND SANITIZING WIPES?
Zhejiang Bright Care Co., Ltd is the labeler of record for SHREK WAFFLE AND SSYRUP HAND SANITIZING WIPES. 16 FDA label records share the active ingredient HAND SANITIZING WIPES, 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 SHREK WAFFLE AND SSYRUP HAND SANITIZING WIPES 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 SHREK WAFFLE AND SSYRUP HAND SANITIZING WIPES 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 HAND SANITIZING WIPES?
Yes. 16 FDA drug label records list HAND SANITIZING WIPES 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 SHREK WAFFLE AND SSYRUP HAND SANITIZING WIPES 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.