Lady Speed Stick

Manufacturer: ALL NATURAL DYNAMICS | Colgate-Palmolive S.A. de C.V.
Effective date: 2013-08-28
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:36:44

Label at a glance#

ProductLady Speed Stick

Active ingredientAluminum Chlorohydrate

Label structure7 sections

Dosage and administration

Apply under arm only. SHAKE WELL BEFORE USE.

Label contents#

Full prescribing information#

Warnings:

WARNINGS SECTION

For External Use Only. Do Not Apply On Irritated Or Injured Skin. Discontinue Use If You Experience Some Irritation, Redness Or Discomfort.

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate 15%

Purpose

OTC - PURPOSE SECTION

Anti Perspirant

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out Of The Reach Of Children

USE:

INDICATIONS & USAGE SECTION

reduces underarm persperation

Directions:

DOSAGE & ADMINISTRATION SECTION

Apply under arm only.

SHAKE WELL BEFORE USE.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, soy oil, steareth-2 PPG-15 stearyl ether, steareth-20, fragrance, caprillglycol, Xanlein, (Xyitol, lemon extract-citrus medicalimonum), fruit extract carica papaya (papaya) olea leaf extract (olive) tetrasodium EDTA and BHT

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51769-666-65	2019-11-27	C162847	48780-1	9855d018-d859-cd31-e053-dbdaa90ab51a	Lady Speed Stick

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
51769-666-65	Lady Speed Stick	65 g in 1 APPLICATOR	STICK	65		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51769-666	LADY SPEED STICK (ALUMINUM CHLOROHYDRATE) STICK [ALL NATURAL DYNAMICS]	1	Legacy NDC, 1 package rows	20130829_0d34a934-b564-4241-8b3a-a0e0e6a747e6.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
Aluminum Chlorohydrate	ACTIVE INGREDIENT	HPN8MZW13M	1
ALUMINUM CHLOROHYDRATE	ACTIVE MOIETY	HPN8MZW13M	1
CITRUS MEDICA FRUIT	INACTIVE INGREDIENT	ZE5Q6PN9ON	1
EDETATE SODIUM	INACTIVE INGREDIENT	MP1J8420LU	1
LEMON	INACTIVE INGREDIENT	24RS0A988O	1
OLEA EUROPAEA LEAF	INACTIVE INGREDIENT	MJ95C3OH47	1
PAPAYA	INACTIVE INGREDIENT	KU94FIY6JB	1
Water	INACTIVE INGREDIENT	059QF0KO0R	1
XYLITOL	INACTIVE INGREDIENT	VCQ006KQ1E	1

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

Lady Speed Stick
Aluminum Chlorohydrate
Water
XYLITOL
LEMON
CITRUS MEDICA FRUIT
PAPAYA
OLEA EUROPAEA LEAF
EDETATE SODIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
51769-666	51769-666-65

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
Aluminum Chlorohydrate	HPN8MZW13M	ACTIB
Water	059QF0KO0R	IACT
XYLITOL	VCQ006KQ1E	IACT
LEMON	24RS0A988O	IACT
CITRUS MEDICA FRUIT	ZE5Q6PN9ON	IACT
PAPAYA	KU94FIY6JB	IACT
OLEA EUROPAEA LEAF	MJ95C3OH47	IACT
EDETATE SODIUM	MP1J8420LU	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 24 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
EDETATE SODIUM	EDETATE SODIUM	MP1J8420LU	SHAMPOO / TOPICAL	1.33 %w/w		Exact identifier — unii candidate 12 equally ranked IID candidates
EDETATE SODIUM	EDETATE SODIUM	MP1J8420LU	SPONGE / TOPICAL	0.14 %w/w		Exact identifier — unii candidate 12 equally ranked IID candidates
XYLITOL	XYLITOL	VCQ006KQ1E	TABLET, ORALLY DISINTEGRATING / ORAL		360 mg	Exact identifier — unii candidate 12 equally ranked IID candidates
XYLITOL	XYLITOL	VCQ006KQ1E	SPRAY / SUBLINGUAL		22 mg	Exact identifier — unii candidate 12 equally ranked IID candidates
XYLITOL	XYLITOL	VCQ006KQ1E	FILM, SOLUBLE / ORAL		29 mg	Exact identifier — unii candidate 12 equally ranked IID candidates
EDETATE SODIUM	EDETATE SODIUM	MP1J8420LU	SOLUTION / OPHTHALMIC	0.1 %w/v		Exact identifier — unii candidate 12 equally ranked IID candidates
EDETATE SODIUM	EDETATE SODIUM	MP1J8420LU	SOAP / TOPICAL	0.12 %w/w		Exact identifier — unii candidate 12 equally ranked IID candidates
XYLITOL	XYLITOL	VCQ006KQ1E	TABLET, FILM COATED, EXTENDED RELEASE / ORAL		72 mg	Exact identifier — unii candidate 12 equally ranked IID candidates
XYLITOL	XYLITOL	VCQ006KQ1E	SUSPENSION / ORAL		1500 mg	Exact identifier — unii candidate 12 equally ranked IID candidates
EDETATE SODIUM	EDETATE SODIUM	MP1J8420LU	TABLET / ORAL	5 mg		Exact identifier — unii candidate 12 equally ranked IID candidates
XYLITOL	XYLITOL	VCQ006KQ1E	POWDER, FOR SUSPENSION / ORAL	4223 mg		Exact identifier — unii candidate 12 equally ranked IID candidates
EDETATE SODIUM	EDETATE SODIUM	MP1J8420LU	INJECTION, SOLUTION / INTRAVENOUS	0.04 %w/v		Exact identifier — unii candidate 12 equally ranked IID candidates
EDETATE SODIUM	EDETATE SODIUM	MP1J8420LU	CAPSULE / ORAL	1 mg		Exact identifier — unii candidate 12 equally ranked IID candidates
EDETATE SODIUM	EDETATE SODIUM	MP1J8420LU	LOTION / TOPICAL	0.17 %w/w		Exact identifier — unii candidate 12 equally ranked IID candidates
EDETATE SODIUM	EDETATE SODIUM	MP1J8420LU	INJECTION / INTRAVENOUS	0.01 %w/v		Exact identifier — unii candidate 12 equally ranked IID candidates
XYLITOL	XYLITOL	VCQ006KQ1E	TABLET / ORAL	15.04 mg		Exact identifier — unii candidate 12 equally ranked IID candidates
EDETATE SODIUM	EDETATE SODIUM	MP1J8420LU	EMULSION / OPHTHALMIC	0.02 %w/v		Exact identifier — unii candidate 12 equally ranked IID candidates
XYLITOL	XYLITOL	VCQ006KQ1E	GUM, CHEWING / BUCCAL		11915 mg	Exact identifier — unii candidate 12 equally ranked IID candidates
XYLITOL	XYLITOL	VCQ006KQ1E	SOLUTION / ORAL		21600 mg	Exact identifier — unii candidate 12 equally ranked IID candidates
XYLITOL	XYLITOL	VCQ006KQ1E	TABLET, EXTENDED RELEASE / ORAL		2752 mg	Exact identifier — unii candidate 12 equally ranked IID candidates
XYLITOL	XYLITOL	VCQ006KQ1E	SUSPENSION, EXTENDED RELEASE / ORAL		9000 mg	Exact identifier — unii candidate 12 equally ranked IID candidates
XYLITOL	XYLITOL	VCQ006KQ1E	PASTE / ORAL		180 mg	Exact identifier — unii candidate 12 equally ranked IID candidates
EDETATE SODIUM	EDETATE SODIUM	MP1J8420LU	INJECTION / INTRAMUSCULAR	0.01 %w/v		Exact identifier — unii candidate 12 equally ranked IID candidates
EDETATE SODIUM	EDETATE SODIUM	MP1J8420LU	SOLUTION / TOPICAL	0.3 %w/w		Exact identifier — unii candidate 12 equally ranked IID candidates

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
4311bbeb-fece-4b8e-80a9-292e0a91befc			0d34a934-b564-4241-8b3a-a0e0e6a747e6	2013-08-28	Warnings	Exact identifier spl id: 4311bbeb-fece-4b8e-80a9-292e0a91befc spl set id: 0d34a934-b564-4241-8b3a-a0e0e6a747e6

Reported adverse events (FAERS/openFDA)#

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