Bloomeffects Tulip Dew Lotion
Product Images NDC 82548-2193

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Bloomeffects Tulip Dew (NDC 82548-2193). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bloomeffects, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Inactive Ingredients (Inactive Ingredients)

Inactive Ingredients (Inactive Ingredients)
Inactive ingredients panel from Bloomeffects Tulip Dew 132 mg/mL shows a list of various substances including water (aqua), alkyl benzoate, caprylic/capric triglyceride, jojoba esters, salicylate derivatives, niacinamide, silica, multiple plant extracts, glycerin, sodium hyaluronate, antioxidants, and several colorants (CI 77499, CI 77492, CI 77491).*
FDA Label Image

Pdp (Pdp)

Pdp (Pdp)
Drug Facts panel for Bloomeffects Tulip Dew sunscreen with 12% Zinc Oxide as the active ingredient. The panel includes uses, warnings, directions, sun protection advice, other information, and a detailed list of inactive ingredients. The text emphasizes skin protection, proper application, and cautions for use.*
FDA Label Image

Directions (Directions)

Directions (Directions)
A drug facts panel with directions and continued drug facts text. Directions advise applying liberally 15 minutes before sun exposure and reapplying after swimming or towel drying. The Sun Protection Measures section recommends reapplication at least every 2 hours, avoiding peak sun hours, wearing protective clothing, and consulting a doctor for children under 6 months. Also instructs to shake well.*
FDA Label Image

Active Ingredients (Drug Facts)

Active Ingredients (Drug Facts)
A partial Drug Facts panel showing the active ingredient Zinc Oxide 12% listed with the purpose Sunscreen. The panel header is bold and titled 'Drug Facts' with columns for Active Ingredient and Purpose.*
FDA Label Image

Uses (Uses)

Uses (Uses)
Text panel showing the 'Uses' section, indicating this product helps prevent sunburn when used as directed along with other sun protection measures, and decreases the risk of skin cancer and early skin aging caused by the sun.*
FDA Label Image

Keep Out Of Reach Of Children (Warning)

Keep Out Of Reach Of Children (Warning)
A warning text panel for external use only product. Instructions include do not use on damaged or broken skin, keep out of eyes and rinse if contact occurs, stop use if skin rash occurs, and keep out of reach of children with instructions for medical assistance if swallowed.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.