amberglow BLEMISH PATCHES
amberglow BLEMISH PATCHES is an FDA drug label for the active ingredient SALICYLIC ACID manufactured by Pearl World Inc. 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 20260727.
- Generic name
- SALICYLIC ACID
- Manufacturer
- Pearl World Inc.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 69933-720
- Application
- M006
- Label effective
- 20260727
About this product
amberglow BLEMISH PATCHES is an FDA-registered drug product whose active ingredient is SALICYLIC ACID. It is labelled by Pearl World Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 69933-720, application M006, label effective 20260727. It is one of 265 FDA drug label records sharing the active ingredient SALICYLIC ACID. 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 SALICYLIC ACID are most often described in connection with: treatment acne. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
USES FOR THE TREATMENT OF ACNE.
Dosage & Administration
DIRECTIONS ADULTS AND CHILDREN OVER 12 YEARS: • CLEAN AND DRY AFFECTED AREA BEFORE APPLICATION. • APPLY PATCH TO BLEMISH AND PRESS FIRMLY FOR 3-5 SECONDS. • LEAVE PATCH ON FOR UP TO 6-8 HOURS. • REMOVE AND REPLACE WITH NEW PATCH AS NEEDED.
Warnings
WARNINGS FOR EXTERNAL USE ONLY. WHEN USING THIS PRODUCT • USING OTHER TOPICAL ACNE MEDICATIONS AT THE SAME TIME OR IMMEDIATELY FOLLOWING USE OF THIS PRODUCT MAY INCREASE DRYNESS OR IRRITATION OF THE SKIN. IF THIS OCCURS, ONLY ONE MEDICATION SHOULD BE USED UNLESS DIRECTED BY A DOCTOR. • AVOID CONTACT WITH EYES. STOP USE AND ASK A DOCTOR IF • IRRITATION OR REDNESS DEVELOPS AND PERSISTS. DO NOT USE • ON IRRITATED OR SUNBURNT SKIN. KEEP OUT OF REACH OF CHILDREN. IF INGESTED GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.
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View labelHow products containing SALICYLIC ACID compare
FDA lists 265 drug label records with SALICYLIC ACID 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 |
|---|---|---|---|
| — | — | L'Oreal USA Products Inc | 20 |
| — | — | Guangzhou Hechuang Commercial Service Co.,Ltd. | 8 |
| — | — | Kenvue Brands LLC | 6 |
| — | — | COSMETIQUE ACTIVE PRODUCTION | 5 |
| — | — | CVS Health | 5 |
Frequently asked questions
What is amberglow BLEMISH PATCHES used for?
USES FOR THE TREATMENT OF ACNE.
Who makes amberglow BLEMISH PATCHES?
Pearl World Inc. is the labeler of record for amberglow BLEMISH PATCHES. 265 FDA label records share the active ingredient SALICYLIC ACID, 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 amberglow BLEMISH PATCHES 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 amberglow BLEMISH PATCHES 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 SALICYLIC ACID?
Yes. 265 FDA drug label records list SALICYLIC ACID 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 amberglow BLEMISH PATCHES 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.