FDA.reportPublic FDA data

Compound hydrolyzed protein beverage

Manufacturer
Nanjing Zhongtiandeheng Applied Stemmedical Co., Ltd | Zhongtian Deheng (Nanjing) Medical Food Co., Ltd
Effective date
2024-12-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:42:49

Label at a glance#

ProductCompound hydrolyzed protein beverage
Active ingredientEGG WHITE
Label structure7 sections

Indications and uses

Treatment of problems caused by diabetes, including： ■high blood sugar ■blood vessel blockage ■liver and kidney function damage ■Hyperglycaemia

Dosage and administration

Adults and children 18 years and over: Direct oral, Once a month, 50ml once Children under 18 years: Prohibited for consumption Direct oral, Once a month, 50ml once

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Egg White 3g

Purpose

OTC - PURPOSE SECTION

Blood vessels health care

Uses

INDICATIONS & USAGE SECTION

Treatment of problems caused by diabetes, including：
■high blood sugar ■blood vessel blockage ■liver and kidney function damage ■Hyperglycaemia

Warnings

WARNINGS SECTION

This product is the same health food, children are not recommended to eat.

Do not use

OTC - DO NOT USE SECTION

■ Can not be used with viral drugs.

■ Can not be used with other cellular preparation..

■ The combination of this product and psychotropic drugs needs to be approved.

■ If pregnant or breastfeeding, consult a health professional before use

When using this product

OTC - WHEN USING SECTION

Wash hands before using

Stop use and ask a doctor

OTC - STOP USE SECTION

if discomfort or unrelieved symptoms occur.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 18 years and over: Direct oral, Once a month, 50ml once
Children under 18 years: Prohibited for consumption
Direct oral, Once a month, 50ml once

Inactive ingredients

INACTIVE INGREDIENT SECTION

CALCIUM CARBONATE, FERROUS SULFATE, LACTALBUMIN, MALTOSE, SUBTILISIN, WATER, ZINC SULFATE

Label 85005-001-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

85005-001-01label85005-001-01label

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
EGG WHITE Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
85005-001-012025-07-29C16284748780-13b156c62-2a13-fb37-e063-e6dba90a4e0785005-001-01

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85005-001-01Compound hydrolyzed protein beverage50 mL in 1 BOTTLELIQUID501
85005-001-01Compound hydrolyzed protein beverage1 in 1 BOXLIQUID11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
85005-001COMPOUND HYDROLYZED PROTEIN BEVERAGE (EGG WHITE) LIQUID [NANJING ZHONGTIANDEHENG APPLIED STEMMEDICAL CO., LTD]12 package rows20241215_2921bf8a-7d3b-79a8-e063-6394a90a513e.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85005-00185005-001-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
MALTOSEXJ6S9RV06FIACT
EGG WHITE3E0I92Z2GRACTIB
FERROUS SULFATE39R4TAN1VTIACT
.ALPHA.-LACTALBUMINGOY102QI5IIACT
ZINC SULFATE89DS0H96TBIACT
WATER059QF0KO0RIACT
CALCIUM CARBONATEH0G9379FGKIACT
SUBTILISIN0ZP13EBC5YIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2921bf8a-7d3c-79a8-e063-6394a90a513e2921bf8a-7d3b-79a8-e063-6394a90a513e2024-12-13WarningsExact identifier
spl id: 2921bf8a-7d3c-79a8-e063-6394a90a513e
spl set id: 2921bf8a-7d3b-79a8-e063-6394a90a513e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.