MIRACLE ATO

Manufacturer: Dr. Ha Skin Lab Co.
Effective date: 2014-10-22
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:40:36

Label at a glance#

ProductMIRACLE ATO

Active ingredientGLYCERIN

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

glycerin

INACTIVE INGREDIENT SECTION

oriental herb ext, green tea ext, adenosine, water, butylene glycol etc

OTC - PURPOSE SECTION

for itching skin, lichenous skin trouble, skin balancing

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out or reach of the children

INDICATIONS & USAGE SECTION

Wash your face with just warm water or a gentle face cleanser and pat dry.
Apply Miracle ATO Moisture Cream to your entire face including the neck area to be needed.
Wait for product to dry completely before going to other steps. Remember to use Miracle ATO daily.

WARNINGS SECTION

- avoid direct sun exposure, keep it refrigerated or in cooler places
- do not eat

DOSAGE & ADMINISTRATION SECTION

for exernal use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
GLYCERIN Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
d676a241-be05-4740-b3ee-1a5f2ed422d2	Product name	4	20180615
dd8bd48f-20d6-43c7-b471-3ae872868afa	Product name	3	20180125
d41954ff-bc63-4b2c-aba0-9146707659d7	Product name	2	20151117

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69309-1001-1	2020-01-31	C162847	48780-1	9d75b9d0-397c-f424-e053-dadaa90a57ce	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69309-1001-1	MIRACLE ATO	80 mL in 1 BOTTLE	CREAM	80		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69309-1001	MIRACLE ATO (GLYCERIN) CREAM [DR. HA SKIN LAB CO.]	1	Legacy NDC, 1 package rows	20141022_9c530e32-1b11-4c1a-97fe-12eeafb733ee.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
GLYCERIN	ACTIVE INGREDIENT	PDC6A3C0OX	1
GLYCERIN	ACTIVE MOIETY	PDC6A3C0OX	1
ADENOSINE	INACTIVE INGREDIENT	K72T3FS567	1
BUTYLENE GLYCOL	INACTIVE INGREDIENT	3XUS85K0RA	1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

MIRACLE ATO
GLYCERIN
ADENOSINE
BUTYLENE GLYCOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
69309-1001	69309-1001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	ACTIB
ADENOSINE	K72T3FS567	IACT
BUTYLENE GLYCOL	3XUS85K0RA	IACT

Source Document#

Source XML · Source PDF

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
BUTYLENE GLYCOL	BUTYLENE GLYCOL	3XUS85K0RA	SYSTEM / TOPICAL		1400 mg	Exact identifier — unii candidate 2 equally ranked IID candidates
BUTYLENE GLYCOL	BUTYLENE GLYCOL	3XUS85K0RA	SYSTEM / TRANSDERMAL	8.12 mg		Exact identifier — unii candidate 2 equally ranked IID candidates

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
5b889b18-4310-44f4-8294-2b99e5a8235e			9c530e32-1b11-4c1a-97fe-12eeafb733ee	2014-10-22	Warnings	Exact identifier spl id: 5b889b18-4310-44f4-8294-2b99e5a8235e spl set id: 9c530e32-1b11-4c1a-97fe-12eeafb733ee

Reported adverse events (FAERS/openFDA)#

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