naturall™ Advanced Hand Sanitizer

Solvall by

Drug Labeling and Warnings

Solvall by is a Otc medication manufactured, distributed, or labeled by Crystal Packaging, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SOLVALL- ethyl alcohol liquid 
Crystal Packaging, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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naturall™ Advanced Hand Sanitizer

Drug Facts

Active Ingredient

Ethyl alcohol 80%

Purpose

Antiseptic

Uses

To decrease bacteria on the skin that could cause disease. Recommended for repeated use.

Warnings

For external use.

Flammable. Keep away from heat or flame.

When using this product. Keep out of eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.

Stop use and ask a doctor if: Irritation and redness develop. condition persists for more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.

Other Information

Do not store between 105°F. May discolor some fabrics. Harmful to wood finishes and plastics.

Inactive Ingredients

Purified water USP, vegetable glycerin, hydrogen peroxide

Kills 99.99% of Most Illness Causing Germs

By Solv-all®

Free of Dyes

Natural Fragrance

Questions? Visit www.SolvAll.com

This Product is free of dyes, added fragrances, triclosan, parabens and preservatives.

Effective at eliminating common germs and bacteria.

This product and its label are in compliance with the regulations set forth by the FDA

Manufactured Exclusively For:

SOLV-ALL®

Beachwood, OH 44122

MADE IN THE USA

Packaging

SOLVALL 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74508-275
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 L  in 100 L

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74508-275-10	3.78 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2020	06/30/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/01/2020	06/30/2021

Labeler - Crystal Packaging, Inc. (160837019)

Establishment
Name	Address	ID/FEI	Business Operations
Crystal Packaging, Inc.		160837019	manufacture(74508-275)

Revised: 8/2021

Document Id: a420ca7b-2431-4797-bc55-5d8417e8c4b7

34390-5

Set id: add588be-ebbc-448a-819e-12537b84d23f

Version: 2

Effective Time: 20210803