FDA.reportPublic FDA data

CL LIGHT

Manufacturer
Powerful X
Effective date
2018-08-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:56:42

Label at a glance#

ProductCL LIGHT
Active ingredientCAFFEINE, GARCINIA GUMMI-GUTTA FRUIT
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Garcinia Cambogia Fruit Extract, Caffeine

INACTIVE INGREDIENT SECTION

Jania Rubens Extract, Laminaria Digitata Extract, Water, etc.

OTC - PURPOSE SECTION

Giving aid to reduce temporary cellulite

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children


WARNINGS SECTION

Consult a physician if you have any abnormal symptoms such as red spots, swelling or itching, or side effects caused by direct sunlight.

DOSAGE & ADMINISTRATION SECTION

for external use only


INDICATIONS & USAGE SECTION

Apply it as a massge befor exercie, after shower.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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
70042-0003-12020-01-31C16284748780-19d75b9d0-0bd4-f424-e053-dadaa90a57ceDrug Facts
70042-0003-22020-01-31C16284748780-19d75b9d0-0bd4-f424-e053-dadaa90a57ceDrug Facts
70042-0003-32020-01-31C16284748780-19d75b9d0-0bd4-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70042-0003-1CL LIGHT2 mL in 1 POUCHCREAM21
70042-0003-2CL LIGHT200 mL in 1 TUBECREAM2001
70042-0003-3CL LIGHT500 mL in 1 BOTTLE, PUMPCREAM5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70042-0003CL LIGHT (GARCINIA GUMMI-GUTTA FRUIT, CAFFEINE) CREAM [POWERFUL X]1Legacy NDC, 3 package rows20180831_74b09d9c-82ad-2bf0-e053-2a91aa0a3388.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70042-000370042-0003-1, 70042-0003-3, 70042-0003-2

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
NameUNIIKind
CAFFEINE3G6A5W338EACTIB
WATER059QF0KO0RIACT
GARCINIA GUMMI-GUTTA FRUITD0QJI8UQVRACTIB

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
74b09d9c-82ae-2bf0-e053-2a91aa0a338874b09d9c-82ad-2bf0-e053-2a91aa0a33882018-08-30WarningsExact identifier
spl id: 74b09d9c-82ae-2bf0-e053-2a91aa0a3388
spl set id: 74b09d9c-82ad-2bf0-e053-2a91aa0a3388

Reported adverse events (FAERS/openFDA)#

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