Newskin Whole-layer Repair Serum Powder For Post-aesthetic Skin Powder
Product Images NDC 87130-001

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Newskin Whole-layer Repair Serum Powder For Post-aesthetic Skin (NDC 87130-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Japan Medical Biotechnology Limited, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

87130-001-01 (87130 001 01)

87130-001-01 (87130 001 01)
Drug Facts panel for NEWSKIN Whole-Layer Repair Serum Powder shows active ingredients Ganoderma Lucidum extract, Schizandra Chinensis seed extract, and Maritime Pine, with purposes including immunomodulator and antioxidant. Includes uses for post-procedure tissue repair and surgical healing support. Provides dosage directions for ages 18-39 and 40-65, warnings, storage instructions, and inactive ingredients. The label is bilingual in English and Chinese and includes manufacturer information and production/expiration dates.*
FDA Label Image

87130-001-02 (87130 001 02)

87130-001-02 (87130 001 02)
Drug Facts panel for NEWSKIN Whole-Layer Repair Serum Powder for Post-Aesthetic Skin lists active ingredients including Ganoderma Lucidum (Mushroom) Extract 2271mg, Schizandra Chinensis Seed Extract 120mg, and Maritime Pine 120mg, with purposes such as immunomodulation and antioxidant support. Directions provide dosing by age. Warnings advise against use in pregnancy, breastfeeding, or allergies. Additional information covers reconstitution, storage, and inactive ingredients, all presented bilingually in English and Chinese.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.