Indications and uses
To help reduce bacteria on the skin
Antimicrobial
- Manufacturer
- VMP Cosmetics
- Effective date
- 2022-01-22
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 23:47:26
Label at a glance#
ProductAntimicrobial
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections
Dosage and administration
Directions * Apply a few sprays directly into the face and bodyas often as needed. Allow to dry without wiping. Safe to spray on clothes. Safe to use all day long.
Storage and handling
Do not store above 104º F.
Label contents#
Full prescribing information#
ACTIVE INGREDIENT
ACTIVE INGREDIENT
Benzalkonium Chloride 0.13%
PURPOSE SECTION
PURPOSE
Antiseptic
USES
To help reduce bacteria on the skin
WARNINGS
For external use only
When using this product
*avoid contact with eyes. If eye contact occurs, flush thoroughly with water.
Stop use
Stop use and consult with a doctor. If irritation or redness develops.
Keep Out of Reach of Children
Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.
Directions
Directions * Apply a few sprays directly into the face and bodyas often as needed. Allow to dry without wiping. Safe to spray on clothes. Safe to use all day long.
Other Information
Do not store above 104º F.
Inactive Ingredients
Agua (Water),Glycerin, Butylene Glycol, Hyaluronic Acid, Aloe Barbadensis Leaf Juice, Echinacea Purpurea, Sambucus Nigra Fruit, GlycyrrhizaUralensis (Licorice), Origanum Vulgare (Oregano) Leaf, HypericumPerforatum, Uncaria Tomentosa, Polysorbate 20, Citric Acid, Tetrasodium EDTA, Ethylhexylglycerin, Phenoxyethanol, Fragrance.
PDP
MEDILAB
365
FACE & BODY SPRAY
ANTI-BACTERIAL
ADVANCED HYDRATING FORMULA
KILLS 99.99%
OF GERMS
3.3 FL. OZ. (100ML)
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 72471-101-10 | 2024-01-30 | C162847 | 48780-1 | 1030e365-09bb-111a-e063-dadaa90a10e2 | af8cc2b4-ef5d-dcaa-e053-2a95a90abb16 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72471-101-10 | Antimicrobial | 1 g in 1 BOTTLE, PLASTIC | LIQUID | 1 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Antimicrobial
- Antimicrobial Face and Body Spray
- ETHYLHEXYLGLYCERIN
- PHENOXYETHANOL
- EUROPEAN ELDERBERRY
- UNCARIA TOMENTOSA LEAF
- POLYSORBATE 20
- CITRIC ACID MONOHYDRATE
- EDETATE SODIUM
- WATER
- ECHINACEA PURPUREA
- OREGANO
- HYPERICUM PERFORATUM
- BENZALKONIUM CHLORIDE
- BENZALKONIUM
- GLYCERIN
- GLYCYRRHIZA URALENSIS
- BUTYLENE GLYCOL
- HYALURONIC ACID
- ALOE VERA LEAF
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 72471-101 | 72471-101-10 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| d626aba9-5955-4a05-e053-2995a90a82d9 | af8cc2b4-ef5d-dcaa-e053-2a95a90abb16 | 2022-01-22 | Warnings | d626aba9-5955-4a05-e053-2995a90a82d9 af8cc2b4-ef5d-dcaa-e053-2a95a90abb16 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.