Dosage and administration
For adults and children of 2 years and over. Children under 2 years ask a doctor before use. Allow to dry without wiping.
CB Alcohol Wipes
- Manufacturer
- Nutritech Pharmaceuticals, Inc
- Effective date
- 2020-03-24
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:09:16
Label at a glance#
ProductCB Alcohol Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections
Label contents#
Full prescribing information#
Active Ingredient
Benzalkonium chloride 0.1%
Purpose
Antibacterial
Use
decreases bacteria on skin
Directions
For adults and children of 2 years and over.
Children under 2 years ask a doctor before use.
Allow to dry without wiping.
Warnings
For external use only.
Do not use
over large areas of the body
if you are allergic to any of the ingredients
when using this product,avoid contact with eyes and face.
If contact occurs,flush thoroughly with water.
Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed, get medical help or contact aPoisonControlCenter right away.
Inactive Ingredients
water,sodium lauryl sulfate,fragrance,2-bromo-2-nitropropane-1,3-diol,aloe barbadensis leaf extract,disodium EDTA,trithanolamine ,glycerin,tocopheryl acetate
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 73529-352-01 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-a4ad-a426-e053-dadaa90af4c2 | a1a6de6b-7fc4-6d0f-e053-2a95a90a13c7 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73529-352-01 | CB Alcohol Wipes | 0.1 g in 1 POUCH | SWAB | 0.1 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- CB Alcohol Wipes
- benzalkonium chloride swab
- ALOE VERA LEAF
- .ALPHA.-TOCOPHEROL ACETATE
- CUPRIC BIS(TRIETHANOLAMINE)
- 2-BROMO-2-NITROETHANOL
- BENZALKONIUM CHLORIDE
- BENZALKONIUM
- WATER
- DISODIUM EDTA-COPPER
- SODIUM LAURYL SULFATE
- GLYCERIN
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 73529-352 | 73529-352-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| .ALPHA.-TOCOPHEROL ACETATE | 9E8X80D2L0 | IACT |
| CUPRIC BIS(TRIETHANOLAMINE) | YBM44X0B6H | IACT |
| 2-BROMO-2-NITROETHANOL | FA22WV2B2Z | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| WATER | 059QF0KO0R | IACT |
| DISODIUM EDTA-COPPER | 6V475AX06U | IACT |
| SODIUM LAURYL SULFATE | 368GB5141J | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
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 |
|---|---|---|---|---|---|---|
| a1a6de6b-7fc5-6d0f-e053-2a95a90a13c7 | a1a6de6b-7fc4-6d0f-e053-2a95a90a13c7 | 2020-03-24 | Warnings | a1a6de6b-7fc5-6d0f-e053-2a95a90a13c7 a1a6de6b-7fc4-6d0f-e053-2a95a90a13c7 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.