dreambeam sunscreen
Generic: sunscreen zinc oxide
Labeler: kosas cosmetics, llcDrug Facts
Product Profile
Brand Name
dreambeam sunscreen
Generic Name
sunscreen zinc oxide
Labeler
kosas cosmetics, llc
Dosage Form
LOTION
Routes
Active Ingredients
zinc oxide 21.7 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
82554-102
Product ID
82554-102_2e097873-ed14-f306-e063-6394a90a1a48
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M020
Listing Expiration
2026-12-31
Marketing Start
2023-04-14
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82554102
Hyphenated Format
82554-102
Supplemental Identifiers
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
dreambeam sunscreen (source: ndc)
Generic Name
sunscreen zinc oxide (source: ndc)
Application Number
M020 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 21.7 g/100mL
Packaging
- 1 TUBE in 1 BOX (82554-102-40) / 40 mL in 1 TUBE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2e097873-ed14-f306-e063-6394a90a1a48", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["f93b0091-6a41-ae6e-e053-6394a90a86d7"], "manufacturer_name": ["Kosas Cosmetics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (82554-102-40) / 40 mL in 1 TUBE", "package_ndc": "82554-102-40", "marketing_start_date": "20230414"}], "brand_name": "DreamBeam Sunscreen", "product_id": "82554-102_2e097873-ed14-f306-e063-6394a90a1a48", "dosage_form": "LOTION", "product_ndc": "82554-102", "generic_name": "Sunscreen Zinc Oxide", "labeler_name": "Kosas Cosmetics, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DreamBeam Sunscreen", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "21.7 g/100mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230414", "listing_expiration_date": "20261231"}