antioxidant sunscreen spf 40

Generic: octinoxate and zinc oxide

Labeler: topiderm, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name antioxidant sunscreen spf 40
Generic Name octinoxate and zinc oxide
Labeler topiderm, inc.
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

octinoxate 75 mg/mL, zinc oxide 70 mg/mL

Manufacturer
Topiderm, Inc.

Identifiers & Regulatory

Product NDC 51326-829
Product ID 51326-829_1e23a07e-f101-477a-98ab-51df88e50464
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2000-07-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51326829
Hyphenated Format 51326-829

Supplemental Identifiers

UNII
4Y5P7MUD51 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 antioxidant sunscreen spf 40 (source: ndc)
Generic Name octinoxate and zinc oxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/mL
  • 70 mg/mL
source: ndc
Packaging
  • 105 mL in 1 BOTTLE, PLASTIC (51326-829-03)
source: ndc

Packages (1)

Ingredients (2)

octinoxate (75 mg/mL) zinc oxide (70 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "1e23a07e-f101-477a-98ab-51df88e50464", "openfda": {"unii": ["4Y5P7MUD51", "SOI2LOH54Z"], "spl_set_id": ["2686378c-8827-47fb-b3ed-07438bd4e9e2"], "manufacturer_name": ["Topiderm, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "105 mL in 1 BOTTLE, PLASTIC (51326-829-03)", "package_ndc": "51326-829-03", "marketing_start_date": "20000728"}], "brand_name": "Antioxidant Sunscreen SPF 40", "product_id": "51326-829_1e23a07e-f101-477a-98ab-51df88e50464", "dosage_form": "LOTION", "product_ndc": "51326-829", "generic_name": "Octinoxate and Zinc Oxide", "labeler_name": "Topiderm, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Antioxidant Sunscreen SPF 40", "active_ingredients": [{"name": "OCTINOXATE", "strength": "75 mg/mL"}, {"name": "ZINC OXIDE", "strength": "70 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20000728", "listing_expiration_date": "20261231"}