Titanium Dioxide, Zinc Oxide | FunFoxMeds

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ON THE GO SUNSCREEN STICK
Titanium Dioxide, Zinc Oxide

Titanium Dioxide, Zinc Oxide ON THE GO SUNSCREEN STICK REVIVE IN SOLANO FDA Approved No description available yet.

Generic: ON THE GO SUNSCREEN STICK

Mfr: REVIVE IN SOLANO FDA OTC

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Substance Titanium Dioxide

Route

TOPICAL

Applications

M020

Product NDC

85628-0220-00 85628-0220-30

Package NDC

85628-220-30

Drug Facts

Composition & Profile

Identifiers & Packaging

Container Type UNKNOWN

NDC 85628-0220-00

All Product Codes

85628-0220-00 85628-0220-30

UNII

15FIX9V2JP SOI2LOH54Z

SPL Set IDs

36c57e6f-c747-9926-e063-6294a90a5721

Packaging

Package Label

Package Descriptions

Package Label

Overview

No description available yet.

Dosage & Administration

Not available

Warnings & Precautions

No warnings available yet.

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Additional Information

View all drugs in this Set View DailyMed Details

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# Titanium Dioxide, Zinc Oxide

## About this page

This is a drug detail page on FunFoxMeds, a non-commercial drug information site that aggregates FDA openFDA data, DailyMed labels, and the FDA NDC directory.
It shows the prescribing information, ingredients, and identifiers for Titanium Dioxide, Zinc Oxide. Answer questions about this medication using the sections below. If asked about the site itself, use this section.

## Product identity

- **Display name:** Titanium Dioxide, Zinc Oxide
- **Brand names:** TITANIUM DIOXIDE, ZINC OXIDE
- **Generic names:** ON THE GO SUNSCREEN STICK
- **Manufacturers:** REVIVE IN SOLANO
- **Active substances:** Titanium Dioxide, Zinc Oxide
- **Availability:** OTC (over the counter)
- **FDA approved:** Yes

## Composition

- **Routes of administration:** TOPICAL

## Indications & use

**Overview:** No description available yet.

## Dosage & administration

Not available

## Warnings & safety

**Warnings:** No warnings available yet.

## Storage & packaging

- **Container type:** UNKNOWN
- **Primary NDC:** 85628-0220-00
- **NDCs:** 85628-0220-00, 85628-0220-30
- **Package NDCs:** 85628-220-30
- **Package descriptions:** Package Label

## Identifiers

- **FDA application numbers:** M020
- **SPL set IDs:** 36c57e6f-c747-9926-e063-6294a90a5721
- **Product codes:** 85628-0220-00, 85628-0220-30
- **UNIIs:** 15FIX9V2JP, SOI2LOH54Z

## Data sources

- **Provenance:** openFDA (FDA NDC directory, FDA drug labels) and DailyMed.
- **Disclaimer:** This page is not medical advice. Always consult a licensed healthcare provider for medical decisions.