RxNorm Names

Review RxNorm Normal Forms

ANTI-BACTERIAL HAND HOME RUN GREEN GRASS (alcohol) gel
[Bath & Body Works, Inc.]

Permanent Link:

http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5e68f437-75b7-4f3e-aab0-e004fbf3355f

Category	DEA Schedule	Marketing Status
HUMAN OTC DRUG LABEL		OTC monograph not final

NOTE: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.

Drug Label Sections

Description
Clinical Pharmacology
Indications & Usage
Contraindications
Warnings
Precautions
Adverse Reactions
Overdosage
Dosage & Administration
How Supplied
Patient Counseling Information
Supplemental Patient Material
Boxed Warning
Patient Package Insert
Highlights
Full Table of Contents
Medication Guide

ACTIVE INGREDIENT

Alcohol 68%

PURPOSE

Antiseptic

USE

Decrease bacteria on hands.

WARNINGS

For external use only.

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water. Stop use and ask a doctor if irritation and redness develop or increase.

FLAMMABLE

Keep away from flame or high heat.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center immediately.

DIRECTIONS

Rub a dime sized drop into hands.

INACTIVE INGREDIENTS

Water (Aqua, Eau), Isopropyl Alcohol, Fragrance (Parfum), Honey Extract (Mel, Extrait de miel), Elaeis Guineensis (Palm) Extract, Cocos Nucifera (Coconut) Fruit Extract, Olea Europaea (Olive) Fruit Extract, Wheat Amino Acids, Retinyl Palmitate, Tocopheryl Acetate, Carbomer, Lactose, Cellulose, Hydroxyethyl Urea, Hydroxypropyl Methylcellulose, Glycerin, Aminomethyl Propanol, Isopropyl Myristate, Propylene Glycol, Ultramarines (CI 77007), Yellow 5 (CI 19140), Blue 1 (CI 42090).

PRODUCT PACKAGING

MM1

ANTI-BACTERIAL HAND HOME RUN GREEN GRASS
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:62670-4414
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (ALCOHOL)	ALCOHOL	68 mL in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER

Packaging
#	Item Code	Package Description
1	NDC:62670-4414-0	29 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/06/2012

Labeler - Bath & Body Works, Inc. (878952845)

Establishment
Name	Address	ID/FEI	Business Operations
Tri-Tech Laboratories, Inc.		792844680	manufacture(62670-4414)

Revised: 01/2013

Document Id: ce2fbf63-8472-47ef-8bfb-0fa7cef425c6

Set id: 5e68f437-75b7-4f3e-aab0-e004fbf3355f

Version: 1

Effective Time: 20130117

Bath & Body Works, Inc.

Daily Med

Current Medication Information

Options

Additional Resources