Novominsyrup Liquid
FDA Label NDC 72988-0034

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Lydia Co., Ltd. for the product Novominsyrup (NDC 72988-0034). 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 otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, inactive ingredient, 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

Otc - Purpose

■ throw up■ whirl ■ headache

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Indications & Usage

■ adult and children 15 years of age and older: 1 pack 30 minutes before boarding.

■ children under 15 years of age: ask a doctor

Warnings

Ask a doctor before use if you have taking a prescription drug.

When using this product

■ Do not take more than 3 pack in 24 hours

■ If you take an additional dose, take it after 4 hours or more

Keep out of reach of children

Inactive Ingredient

concentrated glycerin, malt syrup, high fructose 55

Dosage & Administration

for oral use

Package Label.Principal Display Panel

Label (Label)

Label (Label)

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