DURADRY HANDS AND FEET ANTIPERSPIRANT WIPES- aluminum sesquichlorohydrate cloth

Država: Združene države Amerike

Jezik: angleščina

Source: NLM (National Library of Medicine)

Aktivna sestavina:

ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V) (ALUMINUM SESQUICHLOROHYDRATE - UNII:UCN889409V)

Dostopno od:

AHC Ltd

Pot uporabe:

TOPICAL

Tip zastaranja:

OTC DRUG

Terapevtske indikacije:

Antiperspirant Reduces perspiration

Status dovoljenje:

OTC monograph final

Lastnosti izdelka

DURADRY HANDS AND FEET ANTIPERSPIRANT WIPES- ALUMINUM
SESQUICHLOROHYDRATE CLOTH
AHC LTD
----------
DURADRY HANDS AND FEET ANTIPERSPIRANT WIPES AHC
ACTIVE INGREDIENT
Aluminum Sesquichlorohydrate 20%
PURPOSE
Antiperspirant
USES
Reduces perspiration
WARNINGS
For external use only.
DO NOT USE
on broken skin
ASK A DOCTOR BEFORE USE
if you have kidney disease.
KEEP OUT OF REACH OF CHILDREN
If swallowed, get medical help or contact a Poison Control Center
immediately.
STOP USE
if rash or irritation occurs.
DIRECTIONS
Apply at bedtime. Wash and dry hands/feet thoroughly. Wipe hands/feet
and let air dry.
Wash off the next morning. Apply as needed during the day.
INACTIVE INGREDIENTS
Water, Caprylyl Glycol, Ethylhexylglycerin, Hydroxyacetophenone,
Disodium EDTA,
Sodium Citrate.
QUESTIONS?
Learn more at duradry.com
Dist. by Novadore USA LLC
Miami, FL 33179
DURADRY ANTIPERSPIRANT WIPES (ALUMINUM SESQUICHLOROHYDRATE)
DURADRY HANDS AND FEET ANTIPERSPIRANT WIPES
aluminum sesquichlorohydrate cloth
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:79967-008
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V) (ALUMINUM
SESQUICHLOROHYDRATE - UNII:UCN889409V)
ALUMINUM
SESQUICHLOROHYDRATE
200 mg
in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
EDETATE DISODIUM (UNII: 7FLD91C86K)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
WATER (UNII: 059QF0KO0R)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
PACKAGING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:79967-008-
01
30 in 1 POUCH
03/29/2022
1
155 mL in 1 POUCH; Type 0: Not a Combination
Product
AHC Ltd
MARKETING INFORMATION
MARKETING
CATEGORY
APPLICATION NUMBER OR MONOGRAPH
CITATION
MARKETING START
DATE
MARKETING END
DATE
OTC Monograph Drug
M019
03/29/2022
LABELER -
AHC Ltd (413138557)
REGISTRANT -
AHC Ltd (413138557)
Revised: 1/2024