GlowBiotics Tinted Sunscreen SPF 30

ZINC OXIDE TOPICAL HUMAN OTC DRUG

GlowBiotics Tinted Sunscreen SPF 30 is an FDA drug label for the active ingredient ZINC OXIDE manufactured by Rum Brands, LLC 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 20260616.

Generic name
ZINC OXIDE
Manufacturer
Rum Brands, LLC
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
87788-203
Application
M020
Label effective
20260616

About this product

GlowBiotics Tinted Sunscreen SPF 30 is an FDA-registered drug product whose active ingredient is ZINC OXIDE. It is labelled by Rum Brands, LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87788-203, application M020, label effective 20260616. It is one of 404 FDA drug label records sharing the active ingredient ZINC OXIDE. 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 ZINC OXIDE are most often described in connection with: helps prevent. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredients Purpose Titanuium Dioxide 11% Zinc Oxide 4%

Indications & Usage

Uses helps prevent sunbur

Dosage & Administration

Directions cleanse skin throughly before applying use alone or under make-up apply liberally and evenly 15 minutes before sun exposure reapply at least every 2 hours use a water resistant sunscreen if swimming or sweating Sun Protection Measures. Spending time in the sun increases you risk of cancer and early skin aging. To decrease this risk, regulalry use a sunscreen with a Broad Spectrum SPF value of 15 of higher and other sun protection measures including: limit time in the sun, especially form 10a.m. - 2p.m. wear long-sleeved shirts, pants, hats and sunglasses Children under 6 months, ask doctor.

Warnings

Warnings For external use only. When using this product keep out of eyes. Rinse with water to remove. Stop use and ask doctor if rash occurs .

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How products containing ZINC OXIDE compare

FDA lists 404 drug label records with ZINC OXIDE 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 formProductsManufacturerProducts
— — Ilia, Inc. 30
— — COSMAX USA, CORP 24
— — Colorescience 16
— — Allure Labs Inc 9
— — Raw Elements LLC 9

Frequently asked questions

What is GlowBiotics Tinted Sunscreen SPF 30 used for?
Uses helps prevent sunbur

Who makes GlowBiotics Tinted Sunscreen SPF 30?
Rum Brands, LLC is the labeler of record for GlowBiotics Tinted Sunscreen SPF 30. 404 FDA label records share the active ingredient ZINC OXIDE, 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 GlowBiotics Tinted Sunscreen SPF 30 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 GlowBiotics Tinted Sunscreen SPF 30 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 ZINC OXIDE?
Yes. 404 FDA drug label records list ZINC OXIDE 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 GlowBiotics Tinted Sunscreen SPF 30 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.