Dosage and administration
Wet hands thoroughly with product and allow to dry without wiping. Supervise children under 6 years of age when using this product to avoid swallowing. Not recommended for infants
Wet hands thoroughly with product and allow to dry without wiping. Supervise children under 6 years of age when using this product to avoid swallowing. Not recommended for infants
Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F) May discolor some fabrics Harmful to wood finishes and plastics
Ethyl Alcohol 70%
This is a hand sanitizer manufactured according to the
Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.
The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:
The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.
Antiseptic
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
For external use only. Flammable. Keep away from heat or flame. When using the product, keep out of eyes. Do not inhale or ingest.
on open skin wounds - around eyes - in ears and mouth
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, flush thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Aqua (Water), Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Parfum (Fragrance), Triethanolamine, Aloe Barbadensis Leaf Juice Powder
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 74819-0106-3 | 2024-01-30 | C162847 | 48780-1 | 1030e365-5ed6-111a-e063-dadaa90a10e2 | EUROPEAN SOAPS - 100ml BERG and THYME Hand purifying gel |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 74819-0106-3 | 100ml BERG and THYME Hand purifying | 100 mL in 1 BOTTLE, PLASTIC | GEL | 100 | 1 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 74819-0106 | 100ML BERG AND THYME HAND PURIFYING (ALCOHOL) GEL [LABORATOIRES BEA] | 1 | Legacy NDC, 1 package rows | 20220628_e26f9ea0-cb5a-c4fc-e053-2995a90a0419.zip |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 74819-0106 | 74819-0106-3 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| TROLAMINE | 9O3K93S3TK | IACT |
| ALOE | V5VD430YW9 | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) | 59TL3WG5CO | IACT |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
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 |
|---|---|---|---|---|---|---|
| e26faa95-0388-5133-e053-2995a90a1a27 | e26f9ea0-cb5a-c4fc-e053-2995a90a0419 | 2022-06-27 | Warnings | e26faa95-0388-5133-e053-2995a90a1a27 e26f9ea0-cb5a-c4fc-e053-2995a90a0419 |
Adverse event summaries are temporarily unavailable. Other product information remains available.