PRIMEST HAND SANITIZER Non-Sterile Isopropy Antiseptic Topical Solution

PRIMEST HAND SANITIZER NonSterile Isopropy Antiseptic by

Drug Labeling and Warnings

PRIMEST HAND SANITIZER NonSterile Isopropy Antiseptic by is a Otc medication manufactured, distributed, or labeled by Prime Lab, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PRIMEST HAND SANITIZER NONSTERILE ISOPROPY ANTISEPTIC- isopropyl alcohol gel 
Prime Lab, LLC

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PRIMEST HAND SANITIZER Non-Sterile Isopropy Antiseptic Topical Solution

Drug Facts

Active ingredient(s)

Isopropyl 70% v/v

Purpose

Antiseptic

Use (s)

• Health care personnel hand rub to reduce bacteria that potentially can cause disease.

Warnings

For external use only. Flammable. Keep away from heat or flame.

Do not use

• in children less than 2 months of age
• on open skin wounds

When using this product

Keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask doctor if

• Irritation or rash occurs. These may be signs of serious condition 

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
• Supervise children under 6 years of age when using this product to avoid swallowing

Other information

• Store between 15-30° C (59-86° F)
• Avoid freezing and excessive heat above 40° C (104° F)

Inactive ingredients:

glycerin, aloe vera, purified water, carbopol, triethanolamine, fruit fragrance

Package Labeling:

PRIMEST HAND SANITIZER NONSTERILE ISOPROPY ANTISEPTIC 
isopropyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79937-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79937-010-06	118.25 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/01/2020	01/16/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	11/01/2020	01/16/2024

Labeler - Prime Lab, LLC (117553548)

Revised: 1/2024

Document Id: 0fb28994-6010-1dfa-e063-6394a90adbee

34390-5

Set id: b4035059-c284-3317-e053-2a95a90a57ab

Version: 3

Effective Time: 20240124