shiseido revitalessence skin glow foundation 560

Generic: octinoxate

Labeler: shiseido americas corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name shiseido revitalessence skin glow foundation 560
Generic Name octinoxate
Labeler shiseido americas corporation
Dosage Form EMULSION
Routes
TOPICAL
Active Ingredients

octinoxate 2.30805 g/30mL

Manufacturer
SHISEIDO AMERICAS CORPORATION

Identifiers & Regulatory

Product NDC 58411-895
Product ID 58411-895_42396ecf-8a35-47cf-ae52-a58da9276038
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2023-08-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 58411895
Hyphenated Format 58411-895

Supplemental Identifiers

UNII
4Y5P7MUD51

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 shiseido revitalessence skin glow foundation 560 (source: ndc)
Generic Name octinoxate (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 2.30805 g/30mL
source: ndc
Packaging
  • 1 CONTAINER in 1 CARTON (58411-895-40) / 30 mL in 1 CONTAINER
source: ndc

Packages (1)

58411-895-40 1 CONTAINER in 1 CARTON (58411-895-40) / 30 mL in 1 CONTAINER

Ingredients (1)

octinoxate (2.30805 g/30mL)

Linked Drug Pages (1)

SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 110, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 120, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 130, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 140, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 150, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 160, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 210, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 220, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 230, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 240, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 250, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 260, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 310, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 320, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 330, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 340, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 350, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 360, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 410, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 420, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 430, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 440, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 450, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 460, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 510, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 520, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 530, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 540, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 550, SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 560 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "42396ecf-8a35-47cf-ae52-a58da9276038", "openfda": {"unii": ["4Y5P7MUD51"], "spl_set_id": ["393ce1fa-f188-45d0-a23e-2818de974995"], "manufacturer_name": ["SHISEIDO AMERICAS CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 CONTAINER in 1 CARTON (58411-895-40)  / 30 mL in 1 CONTAINER", "package_ndc": "58411-895-40", "marketing_start_date": "20230801"}], "brand_name": "SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION 560", "product_id": "58411-895_42396ecf-8a35-47cf-ae52-a58da9276038", "dosage_form": "EMULSION", "product_ndc": "58411-895", "generic_name": "OCTINOXATE", "labeler_name": "SHISEIDO AMERICAS CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SHISEIDO REVITALESSENCE SKIN GLOW FOUNDATION", "brand_name_suffix": "560", "active_ingredients": [{"name": "OCTINOXATE", "strength": "2.30805 g/30mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230801", "listing_expiration_date": "20261231"}