78 x 36 spf 30 active
Generic: zinc oxide
Labeler: dermazone llcDrug Facts
Product Profile
Brand Name
78 x 36 spf 30 active
Generic Name
zinc oxide
Labeler
dermazone llc
Dosage Form
CREAM
Routes
Active Ingredients
zinc oxide .2 g/g
Manufacturer
Identifiers & Regulatory
Product NDC
58466-109
Product ID
58466-109_1c2b73fd-1c52-4db3-982e-d937c04ceeac
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M020
Listing Expiration
2026-12-31
Marketing Start
2023-10-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
58466109
Hyphenated Format
58466-109
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
78 x 36 spf 30 active (source: ndc)
Generic Name
zinc oxide (source: ndc)
Application Number
M020 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .2 g/g
Packaging
- 1 TUBE in 1 CARTON (58466-109-03) / 96 g 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": "1c2b73fd-1c52-4db3-982e-d937c04ceeac", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["96a8aacc-5c2f-410a-8fb4-8b3bc0f81e55"], "manufacturer_name": ["Dermazone LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (58466-109-03) / 96 g in 1 TUBE", "package_ndc": "58466-109-03", "marketing_start_date": "20231001"}], "brand_name": "78 x 36 SPF 30 Active", "product_id": "58466-109_1c2b73fd-1c52-4db3-982e-d937c04ceeac", "dosage_form": "CREAM", "product_ndc": "58466-109", "generic_name": "ZINC OXIDE", "labeler_name": "Dermazone LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "78 x 36 SPF 30 Active", "active_ingredients": [{"name": "ZINC OXIDE", "strength": ".2 g/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20231001", "listing_expiration_date": "20261231"}