OTC - ACTIVE INGREDIENT SECTION
Witch Hazel 0.098%
Menthol 0.1%
Caffeine 0.050%
Powerbooster Mild
- 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 22:56:27
Label at a glance#
ProductPowerbooster Mild
Active ingredientWITCH HAZEL, MENTHOL, CAFFEINE
Label structure8 sections
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
Skin Protectant
Cooling
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, Ethyl Hexanediol, Vanillyl Butyl Ether, 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, Citrus Grandis (Grapefruit) Peel Oil, Phyllacantha Fibrosa Extract, Xanthan Gum, Disodium EDTA, Glycolic Acid, 1,2-Hexanediol
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| CAFFEINE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 70843-002-02 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-0e77-a910-e053-dadaa90a0b85 | Drug Facts_70843-002 Powerbooster Mild |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70843-002-01 | Powerbooster Mild | 100 mL in 1 TUBE | CREAM | 100 | 1 | |
| 70843-002-02 | Powerbooster Mild | 1 in 1 CARTON | CREAM | 1 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Powerbooster Mild
- Witch Hazel, Menthol, Caffeine
- WATER
- ISOPROPYL PALMITATE
- BUTYLENE GLYCOL
- CETYL ETHYLHEXANOATE
- STEARIC ACID
- HYDROGENATED POLYDECENE (550 MW)
- CETOSTEARYL ALCOHOL
- GLYCERYL MONOSTEARATE
- GLYCERIN
- POLYSORBATE 60
- SHEA BUTTER
- DIMETHICONE
- VANILLYL BUTYL ETHER
- ETHOHEXADIOL
- PEG-100 STEARATE
- YELLOW WAX
- SORBITAN SESQUIOLEATE
- .ALPHA.-TOCOPHEROL ACETATE
- CARBOXYPOLYMETHYLENE
- TROMETHAMINE
- GLYCERYL MONOCAPRYLATE
- SCUTELLARIA BAICALENSIS ROOT
- SQUALANE
- GLYCYRRHIZA GLABRA
- CITRUS MAXIMA FRUIT RIND OIL
- XANTHAN GUM
- GLYCOLIC ACID
- EDETATE DISODIUM ANHYDROUS
- 1,2-HEXANEDIOL
- WITCH HAZEL
- MENTHOL
- CAFFEINE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 70843-002 | 70843-002-01, 70843-002-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 71eb565f-f905-43ea-e053-2995a90a4949 | b0824a2e-f663-49d8-85dd-733b6b2642d6 | 2018-07-26 | Warnings | 71eb565f-f905-43ea-e053-2995a90a4949 b0824a2e-f663-49d8-85dd-733b6b2642d6 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.