Vitalising Tonic
FDA Label NDC 71276-010

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ulab for the product Vitalising Tonic (NDC 71276-010). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, inactive ingredient, purpose, warnings, keep out of reach of children, indications & usage, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Active ingredients: GLYCERIN 4.6%

Inactive Ingredient

Inactive ingredients: AQUA (WATER), PROPANEDIOL, PEG-40 HYDROGENATED CASTOR OIL, CENTAUREA CYANUS FLOWER WATER, SODIUM ANISATE, SODIUM LEVULINATE, POLYQUATERNIUM-11, PARFUM (FRAGRANCE), SODIUM BENZOATE, OENOTHERA BIENNIS (EVENING PRIMROSE) LEAF EXTRACT, CI 14700 (FD&C RED N°4)

Purpose

Purpose: Skin hydrating and smoothing

Warnings

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

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Indications & Usage

Indications & Usage: Use twice daily

Dosage & Administration

Dosage & Administration: Apply it to your face neck, and decolletage with cotton pads

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