Night Magic

Manufacturer: New Avon LLC
Effective date: 2019-01-01
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-05-31 22:58:55

Label at a glance#

ProductNight Magic Roll-On Anti-Perspirant Deodorant

Active ingredientALUMINUM CHLOROHYDRATE

Label structure7 sections

Contacts and useful links#

PhoneLabel contact1-800-FOR-AVON

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Aluminum Chlorohydrate 14.5%, anhydrous..

OTC - PURPOSE SECTION

Purpose

..Antiperspirant

INDICATIONS & USAGE SECTION

Uses

•reduces underarm perspiration

WARNINGS SECTION

Warnings

For external use only

OTC - DO NOT USE SECTION

Do not use on broken skin

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease

OTC - STOP USE SECTION

Stop use if rash or irritation occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

•apply to underarms only

INACTIVE INGREDIENT SECTION

Inactive ingredients

WATER/EAU, STEARETH-2, PPG-15 STEARYL ETHER, DICAPRYL ADIPATE, PARFUM/FRAGRANCE, STEARETH-20, ISOPROPYL PALMITATE

OTC - QUESTIONS SECTION

Questions?

Call 1-800-FOR-AVON or 1 -800-265-AVON in Canada

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of labelimage of DFB

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
10096-9468-1	2021-01-29	C162847	48780-1	ba0f9c33-4e89-a910-e053-dadaa90a0b85	Night Magic Anti-Perspirant Roll-On Deodorant
10096-9468-2	2021-01-29	C162847	48780-1	ba0f9c33-4e89-a910-e053-dadaa90a0b85	Night Magic Anti-Perspirant Roll-On Deodorant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
10096-9468-1	Night MagicRoll-On Anti-Perspirant Deodorant	50 mL in 1 BOTTLE, DISPENSING	GEL	50		4
10096-9468-2	Night MagicRoll-On Anti-Perspirant Deodorant	75 mL in 1 BOTTLE, DISPENSING	GEL	75		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10096-9468	NIGHT MAGIC ROLL-ON ANTI-PERSPIRANT DEODORANT (ALUMINUM CHLOROHYDRATE) GEL [NEW AVON LLC]	4	Legacy NDC, 2 package rows	20190320_a37076ed-1670-4718-b185-39e7adbf7fa5.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
Aluminum Chlorohydrate	ACTIVE INGREDIENT	HPN8MZW13M	1
Aluminum Chlorohydrate	ACTIVE MOIETY	HPN8MZW13M	1

Products#

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

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

Night Magic Roll-On Anti-Perspirant Deodorant
Aluminum Chlorohydrate
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
10096-9468	10096-9468-1, 10096-9468-2

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
ALUMINUM CHLOROHYDRATE	HPN8MZW13M	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
84794896-2421-5365-e053-2991aa0a4313			a37076ed-1670-4718-b185-39e7adbf7fa5	2019-01-01	Warnings	Exact identifier spl id: 84794896-2421-5365-e053-2991aa0a4313 spl set id: a37076ed-1670-4718-b185-39e7adbf7fa5

Reported adverse events (FAERS/openFDA)#

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