Dosage and administration
Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.
Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.
Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)
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.
Alcohol 72% v/v. Purpose: Antiseptic
Antiseptic, Hand Sanitizer
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 this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes 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.
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.
Water, Carbomer, Aminomethyl Propanol,Butylene Glycol, Glycerin, Aloe Barbadensis Leaf Juice, Isopropyl Myristate, Ethyl Hexanediol, Phenoxyethanol
236mL NDC: 78229-001-00
236ML NDC:78229-002-00
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 78229-001-00 | 2023-07-28 | C162847 | 48780-1 | 0191ceaa-6dc7-198a-e063-dbdaa90aec3e | a75aadcf-eae2-4c72-e053-2995a90ab343 |
| 78229-002-00 | 2023-07-28 | C162847 | 48780-1 | 0191ceaa-6dc7-198a-e063-dbdaa90aec3e | a75aadcf-eae2-4c72-e053-2995a90ab343 |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 78229-001-00 | SANXIDERM Anti-bacterial Hand Gel 8OZ | 236 mL in 1 BOTTLE | GEL | 236 | 1 | |
| 78229-002-00 | SANZIDERM Antiseptic Hand Sanitizer 8OZ | 236 mL in 1 BOTTLE | GEL | 236 | 1 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 78229-001 | SANXIDERM ANTI-BACTERIAL HAND GEL 8OZ (ALCOHOL) GEL SANZIDERM ANTISEPTIC HAND SANITIZER 8OZ (ALCOHOL) GEL [BEAUTY PARTNERS LLC] | 1 | Legacy NDC, 1 package rows | 20200608_a75aadcf-eae2-4c72-e053-2995a90ab343.zip |
| 78229-002 | SANXIDERM ANTI-BACTERIAL HAND GEL 8OZ (ALCOHOL) GEL SANZIDERM ANTISEPTIC HAND SANITIZER 8OZ (ALCOHOL) GEL [BEAUTY PARTNERS LLC] | 1 | Legacy NDC, 1 package rows | 20200608_a75aadcf-eae2-4c72-e053-2995a90ab343.zip |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 78229-001 | 78229-001-00 |
| 78229-002 | 78229-002-00 |
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| a75aae93-26e7-b49a-e053-2995a90a696f | a75aadcf-eae2-4c72-e053-2995a90ab343 | 2020-06-05 | Warnings | a75aae93-26e7-b49a-e053-2995a90a696f a75aadcf-eae2-4c72-e053-2995a90ab343 |
Adverse event summaries are temporarily unavailable. Other product information remains available.