BODY PRESCRIPTIONS Eucalyptus INFUSED WITH VITAMIN E ANTIBACTERIAL HAND

Manufacturer: ENCHANTE ACCESSORIES INC. | Xiamen Afgamarine Biotechnology Co., Ltd.
Effective date: 2020-10-12
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:31:26

Label at a glance#

ProductBODY PRESCRIPTIONS Eucalyptus INFUSED WITH VITAMIN E ANTIBACTERIAL HAND

Active ingredientBENZALKONIUM CHLORIDE

Label structure7 sections

Dosage and administration

Apply a small amount to palms and rub hands together thoroughly

Storage and handling

Do not store above 105F May doscolor some fabrics Harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

■ To help reduce the bacteria on the skin

WARNINGS

WARNINGS SECTION

For external use only

When using this product, keep out of eyes. In case of contact with eyes, flush thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidenta ingestion, seek professional assistance or contact a Poison Control Center immdiately.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply a small amount to palms and rub hands together thoroughly

Other Information

STORAGE AND HANDLING SECTION

Do not store above 105F

May doscolor some fabrics

Harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Cetearyl Alcohol, Mineral Oil, Glyceryl Stearate, PEG 100 Stearate, Glycerin, C13-14 Isoparaffin, Laureth-7, Polyacrylamide, Phenoxyethanol, Benzyl Alcohol, Fragrance (Parfum), Butyrospermum Parkii (Shea) Butter, Citric Acid, Tocopheryl Acetate, Blue 1, Yellow 5

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1046442	benzalkonium chloride 0.13 % Topical Lotion	PSN	1
1046442	benzalkonium chloride 1.3 MG/ML Topical Lotion	SCD	1
1046442	benzalkonium chloride 0.13 % Topical Lotion	SY	1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
c6f86816-7da6-43ea-8c25-ac9758311cc5	Product name	1	20220118
3c386306-c48a-413e-bb69-70cb268496f3	Product name	1	20210727
252e11b6-1a9a-4283-a242-df2c129c496d	Product name	3	20170717
9869efd7-d6dd-0665-5b67-53adbe6ef15e	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
50563-334-01	2022-01-28	C162847	48780-1	d6a99b39-e417-a426-e053-dadaa90af4c2	50563-334/JAS21F15

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
50563-334-01	BODY PRESCRIPTIONS Eucalyptus INFUSED WITH VITAMIN E ANTIBACTERIAL HAND	236.6 mL in 1 BOTTLE	LOTION	236.6		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50563-334	BODY PRESCRIPTIONS EUCALYPTUS INFUSED WITH VITAMIN E ANTIBACTERIAL HAND (BENZALKONIUM CHLORIDE) LOTION [ENCHANTE ACCESSORIES INC.]	1	Legacy NDC, 1 package rows	20201013_04a56adc-3e8e-466c-bc30-892d8fc1d8d3.zip

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

BODY PRESCRIPTIONS Eucalyptus INFUSED WITH VITAMIN E ANTIBACTERIAL HAND
Benzalkonium Chloride
MINERAL OIL
GLYCERYL STEARATE SE
PEG-100 STEARATE
C13-14 ISOPARAFFIN
GLYCERIN
WATER
POLYACRYLAMIDE (1500 MW)
LAURETH-7
PHENOXYETHANOL
BENZYL ALCOHOL
BENZOIC ACID
CITRIC ACID MONOHYDRATE
BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES
.ALPHA.-TOCOPHEROL ACETATE
FD&C BLUE NO. 1
FD&C YELLOW NO. 5
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
50563-334	50563-334-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MINERAL OIL	T5L8T28FGP	IACT
GLYCERYL STEARATE SE	FCZ5MH785I	IACT
PEG-100 STEARATE	YD01N1999R	IACT
C13-14 ISOPARAFFIN	E4F12ROE70	IACT
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT
POLYACRYLAMIDE (1500 MW)	5D6TC4BRWV	IACT
LAURETH-7	Z95S6G8201	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
BENZYL ALCOHOL	LKG8494WBH	IACT
BENZOIC ACID	8SKN0B0MIM	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES	0C9AC7D6XU	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

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
b17ace94-b60f-1355-e053-2995a90a0e88			04a56adc-3e8e-466c-bc30-892d8fc1d8d3	2020-10-12	Warnings	Exact identifier spl id: b17ace94-b60f-1355-e053-2995a90a0e88 spl set id: 04a56adc-3e8e-466c-bc30-892d8fc1d8d3

Reported adverse events (FAERS/openFDA)#

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