blume sunburst sunscreen

Generic: zinc oxide

Labeler: blume
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name blume sunburst sunscreen
Generic Name zinc oxide
Labeler blume
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

zinc oxide 132 mg/mL

Manufacturer
Blume

Identifiers & Regulatory

Product NDC 83656-2106
Product ID 83656-2106_4134b186-b3a0-a307-e063-6394a90a223a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2024-03-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 836562106
Hyphenated Format 83656-2106

Supplemental Identifiers

UNII
SOI2LOH54Z

Packaging Origin

Original Packager
true

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 blume sunburst sunscreen (source: ndc)
Generic Name zinc oxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 132 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (83656-2106-2) / 50 mL in 1 BOTTLE (83656-2106-1)
source: ndc

Packages (1)

83656-2106-2 1 BOTTLE in 1 CARTON (83656-2106-2) / 50 mL in 1 BOTTLE (83656-2106-1)

Ingredients (1)

zinc oxide (132 mg/mL)

Linked Drug Pages (1)

Blume Sunburst Sunscreen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4134b186-b3a0-a307-e063-6394a90a223a", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["21ef2c6b-8ae7-8bcf-e063-6294a90ae9e1"], "manufacturer_name": ["Blume"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (83656-2106-2)  / 50 mL in 1 BOTTLE (83656-2106-1)", "package_ndc": "83656-2106-2", "marketing_start_date": "20240301"}], "brand_name": "Blume Sunburst Sunscreen", "product_id": "83656-2106_4134b186-b3a0-a307-e063-6394a90a223a", "dosage_form": "LOTION", "product_ndc": "83656-2106", "generic_name": "Zinc Oxide", "labeler_name": "Blume", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Blume Sunburst Sunscreen", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "132 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240301", "listing_expiration_date": "20261231"}