sunsolve md correct and fade

Generic: zinc oxide

Labeler: sunsolve md inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name sunsolve md correct and fade
Generic Name zinc oxide
Labeler sunsolve md inc
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

zinc oxide 132 mg/mL

Manufacturer
Sunsolve MD Inc

Identifiers & Regulatory

Product NDC 84878-200
Product ID 84878-200_4395a3a6-6fe6-e6b9-e063-6294a90ae938
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2024-11-06

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 84878200
Hyphenated Format 84878-200

Supplemental Identifiers

UPC
5061023120033
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 sunsolve md correct and fade (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, PUMP in 1 CARTON (84878-200-02) / 48 mL in 1 BOTTLE, PUMP (84878-200-01)
source: ndc

Packages (1)

84878-200-02 1 BOTTLE, PUMP in 1 CARTON (84878-200-02) / 48 mL in 1 BOTTLE, PUMP (84878-200-01)

Ingredients (1)

zinc oxide (132 mg/mL)

Linked Drug Pages (1)

Sunsolve MD Correct and Fade ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4395a3a6-6fe6-e6b9-e063-6294a90ae938", "openfda": {"upc": ["5061023120033"], "unii": ["SOI2LOH54Z"], "spl_set_id": ["26f3ad9f-f8ca-05d4-e063-6394a90ad5c4"], "manufacturer_name": ["Sunsolve MD Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PUMP in 1 CARTON (84878-200-02)  / 48 mL in 1 BOTTLE, PUMP (84878-200-01)", "package_ndc": "84878-200-02", "marketing_start_date": "20241106"}], "brand_name": "Sunsolve MD Correct and Fade", "product_id": "84878-200_4395a3a6-6fe6-e6b9-e063-6294a90ae938", "dosage_form": "LOTION", "product_ndc": "84878-200", "generic_name": "Zinc Oxide", "labeler_name": "Sunsolve MD Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sunsolve MD Correct and Fade", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "132 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20241106", "listing_expiration_date": "20261231"}