FDA.reportPublic FDA data

Powerbooster Original

Manufacturer
Peterpanlab | ATEC Co., Ltd.
Effective date
2018-07-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:56:26

Label at a glance#

ProductPowerbooster Original
Active ingredientWITCH HAZEL, CAFFEINE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Witch Hazel 0.098%

Caffeine 0.01%

OTC - PURPOSE SECTION

Skin Protectant

Slimming

INDICATIONS & USAGE SECTION

Helps skin moiturizing, cooling and body slimming

DOSAGE & ADMINISTRATION SECTION

1. Excluding face or other sensitive, apply an appropriate amount on the desired area and give a massage.
2. On the first trial, try only a small amount and increase amount for better effects. Control amount to the desired level of heat.

WARNINGS SECTION

For external use only.
Do not use on damaged or broken skin.Stop using and ask a doctor if rash occurs.
When using this product, keep out of eyes. Rinse with water to remove.

If pregnent or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away.

INACTIVE INGREDIENT SECTION

Water, Isopropyl Palmitate, Butylene Glycol, Cetyl Ethylhexanoate, Stearic Acid, Hydrogenated Polydecene, Cetearyl Alcohol, Glyceryl Stearate, Glycerin, Polysorbate 60, Butyrospermum Parkii (Shea) Butter, Dimethicone, Vanillyl Butyl Ether, Ethyl Hexanediol, PEG-100 Stearate, Beeswax, Sorbitan Sesquioleate, Tocopheryl Acetate, Carbomer, Tromethamine, Glyceryl Caprylate, Scutellaria Baicalensis Root Extract, Paeonia Suffruticosa Root Extract, Glycyrrhiza Glabra (Licorice) Root Extract, , Squalane, Fragrance, Xanthan Gum, Disodium EDTA, Glycolic Acid, 1,2-Hexanediol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CAFFEINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
77dc03a4-fbfc-e6a3-fe95-285bbae40d75Product name220250814
7dea7767-9f52-b60a-5435-33cb9cc28baeProduct name420250124
6338270f-96cb-0ecb-6fbb-0a9bc78001f4Product name720250116
0ca83774-3f79-b837-5d6f-c210102f3bc8Product name620250114
41b814f3-0166-1c53-c9ef-a0794c7daf9dProduct name320221110
a590be26-846c-8659-a5a1-fb25907965dcProduct name220221110
2dc76302-91c0-4c35-ad78-99adfb049c4bProduct name120200603
e6065d4b-5ae1-476f-a40e-f2851cbb5d2bProduct name220180221
f212291f-05fe-9603-fc7e-bd73e38ce1e6Product name220161129
182f9ab4-4ab5-c449-200f-87ce2ce8e550Product name220151105
332e86c3-7875-ca6e-f934-2206d2b31996Product name120140508
56625fcc-aa34-9d30-d0e9-1c1beb37ea21Product name120140508
7dfac40f-a405-cd2e-7c06-3059ec0e1092Product name120140508
96c2be53-8e44-452d-56a2-d255b2f1af2dProduct name120140508
bf8bd5f7-495f-4022-2780-7ded7ea7ea44Product name120140508
d223c173-c39b-d764-47d4-d671d3088815Product name120140508
e01133ad-4dcd-c7f3-454b-2ff569ee160aProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70843-001-022021-01-29C16284748780-1ba0f9c33-5627-a910-e053-dadaa90a0b85Drug Facts_70843-001 Powerbooster Original

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70843-001-01Powerbooster Original100 mL in 1 TUBECREAM1001
70843-001-02Powerbooster Original1 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70843-001POWERBOOSTER ORIGINAL (WITCH HAZEL, CAFFEINE) CREAM [PETERPANLAB]1Legacy NDC, 2 package rows20180726_320191f6-c5cd-4728-8c14-a48ae3f549bb.zip

Products#

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

DailyMed product names page 1 of 1 · 31 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70843-00170843-001-01, 70843-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 29 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ISOPROPYL PALMITATE8CRQ2TH63MIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
CETYL ETHYLHEXANOATE134647WMX4IACT
STEARIC ACID4ELV7Z65APIACT
HYDROGENATED POLYDECENE (550 MW)U333RI6EB7IACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
GLYCERINPDC6A3C0OXIACT
POLYSORBATE 60CAL22UVI4MIACT
SHEA BUTTERK49155WL9YIACT
DIMETHICONE92RU3N3Y1OIACT
VANILLYL BUTYL ETHERS2ULN37C9RIACT
ETHOHEXADIOLM9JGK7U88VIACT
PEG-100 STEARATEYD01N1999RIACT
YELLOW WAX2ZA36H0S2VIACT
SORBITAN SESQUIOLEATE0W8RRI5W5AIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
CARBOXYPOLYMETHYLENE0A5MM307FCIACT
TROMETHAMINE023C2WHX2VIACT
GLYCERYL MONOCAPRYLATETM2TZD4G4AIACT
SCUTELLARIA BAICALENSIS ROOT7J95K7ID2SIACT
SQUALANEGW89575KF9IACT
XANTHAN GUMTTV12P4NEEIACT
GLYCOLIC ACID0WT12SX38SIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
WITCH HAZEL101I4J0U34ACTIB
CAFFEINE3G6A5W338EACTIB

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
71eb565f-f8fb-43ea-e053-2995a90a4949320191f6-c5cd-4728-8c14-a48ae3f549bb2018-07-26WarningsExact identifier
spl id: 71eb565f-f8fb-43ea-e053-2995a90a4949
spl set id: 320191f6-c5cd-4728-8c14-a48ae3f549bb

Reported adverse events (FAERS/openFDA)#

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