Dosage and administration
Apply onto dry hands. Work into a lather, rinse and dry thoroughly.
CVS PHARMACY
- Manufacturer
- CVS PHARMACY | APOLLO HEALTH AND BEAUTY CARE
- Effective date
- 2016-02-10
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-05-31 22:44:55
Label at a glance#
ProductCVS PHARMACY COCONUT WATER
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections
Storage and handling
Store at room temperature.
Label contents#
Full prescribing information#
Active ingredient
Benzalkonium Chloride 0.13%
Purpose
Antibacterial
Use
- 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 develop and last.
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, rinse and dry thoroughly.
Other information
- Store at room temperature.
Inactive ingredients
Aloe Barbadensis Leaf Juice, Blue 1 (CI 42090), Camellia Sinensis Leaf Extract, Citric Acid, Cocamidopropyl Betaine, Decyl Glucoside, Fragrance (Parfum), Glycerin, Methylchloroisothiazolinone, Methylisothiazolinone, Polyquaternium-7, Polysorbate 20, Red 33 (CI 17200), Sodium Citrate, Tetrasodium EDTA, Water (Aqua), Xanthan Gum
Label Copy
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 1046593 | benzalkonium chloride 0.13 % Medicated Liquid Soap | PSN | 3 |
| 1046593 | benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap | SCD | 3 |
| 1046593 | benzalkonium chloride 0.13 % Medicated Liquid Soap | SY | 3 |
| 1046593 | benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap | SY | 3 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 59779-842-31 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-0e16-f424-e053-dadaa90a57ce | DRUG FACTS |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 59779-842-31 | CVS PHARMACYCOCONUT WATER | 946 mL in 1 BOTTLE | LIQUID | 946 | 3 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- CVS PHARMACY COCONUT WATER
- BENZALKONIUM CHLORIDE
- BENZALKONIUM
- ALOE VERA LEAF
- BAMBUSA VULGARIS LEAF
- FD&C BLUE NO. 1
- CITRIC ACID MONOHYDRATE
- COCAMIDOPROPYL BETAINE
- DECYL GLUCOSIDE
- GLYCERIN
- METHYLCHLOROISOTHIAZOLINONE
- METHYLISOTHIAZOLINONE
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW)
- POLYSORBATE 20
- D&C RED NO. 33
- SODIUM CITRATE
- EDETATE SODIUM
- WATER
- XANTHAN GUM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 59779-842 | 59779-842-31 |
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 |
|---|---|---|---|---|---|---|
| e6e0aa6a-56cb-4cb1-a59e-df1fef8f7c55 | c31fd094-9f4d-4154-a1a3-ffbcd4243a41 | 2016-02-10 | Warnings | e6e0aa6a-56cb-4cb1-a59e-df1fef8f7c55 c31fd094-9f4d-4154-a1a3-ffbcd4243a41 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.