sjolie tanning spf 30 sunscreen
Generic: zinc oxide
Labeler: sjolie, inc.Drug Facts
Product Profile
Brand Name
sjolie tanning spf 30 sunscreen
Generic Name
zinc oxide
Labeler
sjolie, inc.
Dosage Form
CREAM
Routes
Active Ingredients
zinc oxide 11 g/100g
Manufacturer
Identifiers & Regulatory
Product NDC
85947-001
Product ID
85947-001_3a2943a0-8ac8-d8d5-e063-6394a90a53b7
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M020
Listing Expiration
2026-12-31
Marketing Start
2025-02-27
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
85947001
Hyphenated Format
85947-001
Supplemental Identifiers
UPC
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
sjolie tanning spf 30 sunscreen (source: ndc)
Generic Name
zinc oxide (source: ndc)
Application Number
M020 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 11 g/100g
Packaging
- 177 g in 1 TUBE (85947-001-06)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3a2943a0-8ac8-d8d5-e063-6394a90a53b7", "openfda": {"upc": ["0851397008823"], "unii": ["SOI2LOH54Z"], "spl_set_id": ["3a283a09-2edb-f92c-e063-6294a90a82bd"], "manufacturer_name": ["SJOLIE, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "177 g in 1 TUBE (85947-001-06)", "package_ndc": "85947-001-06", "marketing_start_date": "20250227"}], "brand_name": "Sjolie Tanning SPF 30 Sunscreen", "product_id": "85947-001_3a2943a0-8ac8-d8d5-e063-6394a90a53b7", "dosage_form": "CREAM", "product_ndc": "85947-001", "generic_name": "Zinc Oxide", "labeler_name": "SJOLIE, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sjolie Tanning SPF 30 Sunscreen", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "11 g/100g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250227", "listing_expiration_date": "20261231"}