EQUATE ANTIBACTERIAL FOAMING HAND SPRING SHOWERS- benzalkonium chloride liquid

United States - English - NLM (National Library of Medicine)

Buy It Now

Active ingredient:
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)
Available from:
Wal-Mart Stores Inc
INN (International Name):
BENZALKONIUM CHLORIDE
Composition:
BENZALKONIUM CHLORIDE 1.3 mg in 1 mL
Administration route:
TOPICAL
Prescription type:
OTC DRUG
Therapeutic indications:
- helps eliminate bacteria on the skin.
Authorization status:
OTC monograph not final
Authorization number:
49035-014-07, 49035-014-33

EQUATE ANTIBACTERIAL FOAMING HAND SPRING SHOWERS- benzalkonium

chloride liquid

Wal-Mart Stores Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they

comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Drug Facts

Active ingredient

Benzalkonium Chloride 0.13%

Purpos e

Antibacterial

Us es

helps eliminate bacteria on the skin.

Warnings

For external use only.

When using this product

avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop using this product and ask doctor

if irritation and redness develops and lasts.

Keep out of reach of children.

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

Apply onto dry hands, work into a lather and rinse thoroughly.

Other information

store at room temperature.

Inactive ingredients

Water (Aqua), Cocamidopropyl Betaine, Polysorbate 20, Fragrance (Parfum), Glycerin, Decyl

Glucoside, Hydroxyethylcellulose, Aloe Barbadensis Leaf Juice, Camellia Sinensis Leaf Extract,

Propylene Glycol, Polyquaternium-7, Tetrasodium EDTA, Sodium Citrate, Citric Acid, Benzophenone-

4, Methylchloroisothiazolinone, Methylisothiazolinione, Blue 1 (CI 42090), Ext. Violet 2 (CI 60730).

Label Copy

EQUATE ANTIBACTERIAL FOAMING HAND SPRING SHOWERS

benzalkonium chloride liquid

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:49 0 35-0 14

Route of Administration

TOPICAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

BENZALKO NIUM CHLO RIDE (UNII: F5UM2KM3W7) (BENZALKONIUM -

UNII:7N6 JUD5X6 Y)

BENZALKONIUM

CHLORIDE

1.3 mg

in 1 mL

Inactive Ingredients

Ingredient Name

Stre ng th

WATER (UNII: 0 59 QF0 KO0 R)

CO CAMIDO PRO PYL BETAINE (UNII: 5OCF3O11KX)

PO LYSO RBATE 2 0 (UNII: 7T1F30 V5YH)

GLYCERIN (UNII: PDC6 A3C0 OX)

DECYL GLUCO SIDE (UNII: Z17H9 7EA6 Y)

HYDRO XYETHYL CELLULO SE ( 50 0 0 CPS AT 1%) (UNII: X70 SE6 2ZAR)

ALO E VERA LEAF (UNII: ZY8 1Z8 3H0 X)

GREEN TEA LEAF (UNII: W2ZU1RY8 B0 )

Wal-Mart Stores Inc

PRO PYLENE GLYCO L (UNII: 6 DC9 Q16 7V3)

PO LYQ UATERNIUM-7 ( 7 0 /3 0 ACRYLAMIDE/DADMAC; 16 0 0 0 0 0 MW) (UNII: 0 L414VCS5Y)

EDETATE SO DIUM (UNII: MP1J8 420 LU)

SO DIUM CITRATE (UNII: 1Q73Q2JULR)

CITRIC ACID MO NO HYDRATE (UNII: 29 6 8 PHW8 QP)

SULISO BENZO NE (UNII: 1W6 L6 29 B4K)

METHYLCHLO RO ISO THIAZO LINO NE (UNII: DEL7T5QRPN)

METHYLISO THIAZO LINO NE (UNII: 229 D0 E1QFA)

FD&C BLUE NO . 1 (UNII: H3R47K3TBD)

EXT. D&C VIO LET NO . 2 (UNII: G5UX3K0 728 )

Packag ing

#

Item Code

Package Description

Marketing Start

Date

Marketing End

Date

1

NDC:49 0 35-0 14-

222 mL in 1 BOTTLE, PLASTIC; Type 0 : No t a Co mbinatio n

Pro duc t

0 4/13/20 17

2

NDC:49 0 35-0 14-

9 46 mL in 1 BOTTLE, PLASTIC; Type 0 : No t a Co mbinatio n

Pro duc t

0 4/13/20 17

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

OTC mo no graph no t final

pa rt333E

0 4/13/20 17

Labeler -

Wal-Mart Stores Inc (051957769)

Registrant -

Apollo Health and Beauty Care Inc. (201901209)

Establishment

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

Apo llo Health and Beauty Care Inc.

20 19 0 120 9

ma nufa c ture (49 0 35-0 14)

Revised: 4/2017

Similar products

Search alerts related to this product

Share this information