DURADRY HANDS AND FEET ANTIPERSPIRANT WIPES- aluminum sesquichlorohydrate cloth

국가: 미국

언어: 영어

출처: NLM (National Library of Medicine)

유효 성분:

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

제공처:

Novadore USA Inc

관리 경로:

TOPICAL

처방전 유형:

OTC DRUG

치료 징후:

Antiperspirant Reduces perspiration

승인 상태:

OTC monograph final

제품 특성 요약

DURADRY HANDS AND FEET ANTIPERSPIRANT WIPES- ALUMINUM
SESQUICHLOROHYDRATE CLOTH
NOVADORE USA INC
----------
DURADRY HANDS AND FEET ANTIPERSPIRANT WIPES
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:69990-400
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:69990-400-
01
30 in 1 POUCH
03/29/2022
1
155 mL in 1 POUCH; Type 0: Not a Combination
Product
Novadore USA Inc
MARKETING INFORMATION
MARKETING
CATEGORY
APPLICATION NUMBER OR MONOGRAPH
CITATION
MARKETING START
DATE
MARKETING END
DATE
OTC Monograph Drug
M019
03/29/2022
LABELER -
Novadore USA Inc (079777451)
REGISTRANT -
Novadore USA Inc (079777451)
Revised: 1/2024