STRAIGHT SHOT

Manufacturer: Shift Packaging, LLC
Effective date: 2020-11-06
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:33:08

Label at a glance#

ProductSTRAIGHT SHOT

Active ingredientISOPROPYL ALCOHOL

Label structure9 sections

Indications and uses

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

Dosage and administration

■ Place enough product on hands to cover all surfaces. Rub hands together until dry. ■ Supervise children under 6 years of age when using this product to avoid swallowing.

Contacts and useful links#

PhonePoison Help1-800-222-1222

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 70% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

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 a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Place enough product on hands to cover all surfaces. Rub hands together until dry.
■ Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

SPL UNCLASSIFIED SECTION

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

Inactive Ingredient

INACTIVE INGREDIENT SECTION

water

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
808520	isopropyl alcohol 70 % Topical Solution	PSN	1
808520	isopropyl alcohol 0.7 ML/ML Topical Solution	SCD	1
808520	isopropyl alcohol 70 % Topical Solution	SY	1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79170-003-01	2022-01-28	C162847	48780-1	d6a99b39-989b-a426-e053-dadaa90af4c2	STRAIGHT SHOT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79170-003-01	STRAIGHT SHOT	3785 mL in 1 PACKAGE	LIQUID	3785		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79170-003	STRAIGHT SHOT (ISOPROPYL ALCOHOL) LIQUID [SHIFT PACKAGING, LLC]	1	Legacy NDC, 1 package rows	20201107_3c53bd3b-9835-4106-8398-232d59e19ebf.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

STRAIGHT SHOT
ISOPROPYL ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79170-003	79170-003-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ISOPROPYL ALCOHOL	ND2M416302	ACTIB
WATER	059QF0KO0R	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
0a27007f-2639-44df-90d3-2620974f088d			3c53bd3b-9835-4106-8398-232d59e19ebf	2020-11-06	Warnings	Exact identifier spl id: 0a27007f-2639-44df-90d3-2620974f088d spl set id: 3c53bd3b-9835-4106-8398-232d59e19ebf

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.