HYDRA C3 TRIPLE RESET

Manufacturer
ULAB | U-LAB Switzerland AG
Effective date
2017-03-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:49:20

Label at a glance#

ProductHYDRA C3 TRIPLE RESET
Active ingredientWITCH HAZEL
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: WITCH HAZEL 5.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients: Aqua (WATER), Glycerin (and) Glyceryl Polyacrylate, Bifida Ferment Lysate, Glycerin, Propylene Glycol, Phenoxyethanol, Carbomer, Triethanolamine, Olive Glycerides, Ceramide 3, Fragrance, Mica, CI 77891, Silica, Ethylhexylglycerin, CI 77491, Tin oxide

PURPOSE

OTC - PURPOSE SECTION

Purpose: Skin nourishing and strengthening

WARNINGS

WARNINGS SECTION

Warnings: For external use only Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Indications & Usage: Apply morning and night

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage & Administration: Apply morning and night to face and neck after serum and ampoule

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71276-100-022020-01-31C16284748780-19d75b9cf-fe21-f424-e053-dadaa90a57ce74476689-b618-4d7a-a82a-5bc0357ea32c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71276-100-01HYDRA C3 TRIPLE RESET60 mL in 1 BOTTLE, PUMPCREAM601
71276-100-02HYDRA C3 TRIPLE RESET1 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71276-100HYDRA C3 TRIPLE RESET (WITCH HAZEL) CREAM [ULAB]1Legacy NDC, 2 package rows20170322_74476689-b618-4d7a-a82a-5bc0357ea32c.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71276-10071276-100-01, 71276-100-02

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
WITCH HAZEL101I4J0U34ACTIB
WATER059QF0KO0RIACT
GlycerinPDC6A3C0OXIACT

Source Document#

Source XML · Source PDF

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
f8a723fb-dfb4-49ad-b52d-0f812825214e74476689-b618-4d7a-a82a-5bc0357ea32c2017-03-22WarningsExact identifier
spl id: f8a723fb-dfb4-49ad-b52d-0f812825214e
spl set id: 74476689-b618-4d7a-a82a-5bc0357ea32c

Reported adverse events (FAERS/openFDA)#

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