OTC Medication Information: LUCKY SUPER SOFT FOAMING

LUCKY SUPER SOFT FOAMING- benzalkonium chloride soap
Delta Brands, 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.

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Use

for hand washing to decrease bacteria on the skin

Warnings

For external use only

When using this product

avoid contact with the eyes. In case of eye contact, flush with water.

Stop use and ask a doctor if

irritation and redness develops

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

■ wet hands and apply soap ■ lather all surfaces of hands and fingers by rubbing vigorously for at least 20 seconds ■ rinse hands well and dry

Inactive ingredients

water, glycerin, lauramine oxide, cetrimonium chloride, cocamidopropyl betaine, decyl glucoside, hydroxypropyl methylcellulose, fragrance, zinc sulfate, citric acid, sodium chloride, tetrasodium EDTA, alcohol, methylchloroisothiazolinone, methylisothiazolinone

Package Label

package label
(click image for full-size original)

LUCKY SUPER SOFT FOAMING
benzalkonium chloride soap
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:20276-138
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 0.13 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER
DECYL GLUCOSIDE
LAURAMINE OXIDE
GLYCERIN
CETRIMONIUM CHLORIDE
COCAMIDOPROPYL BETAINE
HYPROMELLOSE, UNSPECIFIED
ZINC SULFATE
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
EDETATE SODIUM
CITRIC ACID MONOHYDRATE
SODIUM CHLORIDE
ALCOHOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:20276-138-75 222 mL in 1 BOTTLE, PUMP None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 01/29/2021
Labeler — Delta Brands, Inc (102672008)

Revised: 06/2023 Delta Brands, Inc

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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