Guard
Guard is an FDA drug label for the active ingredient ALCOHOL manufactured by Apollo Health and Beauty Care administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260505.
- Generic name
- ALCOHOL
- Manufacturer
- Apollo Health and Beauty Care
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 63148-502
- Application
- 505G(a)(3)
- Label effective
- 20260505
About this product
Guard is an FDA-registered drug product whose active ingredient is ALCOHOL. It is labelled by Apollo Health and Beauty Care taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 63148-502, application 505G(a)(3), label effective 20260505. It is one of 582 FDA drug label records sharing the active ingredient ALCOHOL. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing ALCOHOL are most often described in connection with: personal hand, hygine help, spread bacteria, washing soap. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses For personal hand hygine to help prevent the spread of bacteria, and can be used in place of hand washing if soap and water are not available.
Dosage & Administration
Directions For occassional and Personal use. Rub thoroughly into hands for at least 30 seconds. Allo to dry. Children under 6 years should be supervised when using this product.
Warnings
Warnings For external use only. Flammable Keep away from source of heat or fire. Do not use On infants less than 2 months of age. On open skin wounds On broken or damaged skin. When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. Do not inhale. Stop use and ask a doctor if irritation or redness develops and lasts. Keep out of reach of children In case of accidental ingestion, get medical help or contact Poison Control Center immediately.
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View labelHow products containing ALCOHOL compare
FDA lists 582 drug label records with ALCOHOL as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Bath & Body Works, Inc. | 79 |
| — | — | Shenzhen Lantern Scicence Co.,Ltd. | 66 |
| — | — | Fourstar Group USA, Inc. | 41 |
| — | — | Church & Dwight Co., Inc. | 33 |
| — | — | Target Corporation | 23 |
Recall and safety notices
5 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.
| Recall | Product | Firm | Class | Status | Reported |
|---|---|---|---|---|---|
| D-0663-2026 | Medline Remedy Specialized Silicone Cream (Hydraguard-D ),Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL 80090 2 FL OZ (59 mL) NDC 53329-159-13 4 FL OZ (118 mL) NDC 53329-159-04 | BioMed Laboratories, LLC. | Class II | Ongoing | 20260715 |
| D-0557-2026 | KIRKLAND Signature, ULTRA STRENGTH ANTACID, Calcium Carbonate, 1000 mg, 265-count bottle, MANUFACTURED BY: GUARDIAN DRUG COMPANY, INC., 2 CHARLES COURT/DAYTON, NJ 08810, FOR: Costco Wholesale Corporation, 999 Lake Drive, Issaquah, WA 98027, NDC 63981-171-80 | Guardian Drug Co. Inc. | Class II | Ongoing | 20260610 |
| D-0374-2026 | Green Guard Antiseptic Wipes (Benzalkonium Chloride 0.13%), 25 wipes per box, Distributed by Green Guard, St. Louis, MO 63045, NDC 47682-056-73 | ACME UNITED CORPORATION | Class II | Ongoing | 20260311 |
| D-0173-2026 | PeriGuard Ointment, Petrolatum 49.9%, packaged in a) 5g (NDC 61924-205-05), b) 3.5oz (NDC 61924-205-04), and c) 7oz (NDC 61924-205-07) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. | DermaRite Industries, LLC | Class II | Ongoing | 20251126 |
| D-0218-2025 | Granix (tbo-filgrastim) Injection 300 mcg/0.5 mL, Single Dose prefilled syringe, packaged as a) 1 syringe in 1 CARTON, NDC 63459-910-11, Blister NDC 63459-910-12; (b)10 syringes in 1 CARTON, NDC 63459-910-15, Blister NDC 63459-910-12; (c) 1 syringe in 1 CARTON, NDC 63459-910-17 without safety guard and blister, Rx Only, Manufactured by: UAB Teva Baltics, Vilnius, Lithuania. Distributed by Teva Pharmaceuticals USA, Inc. North Wales PA 19454. Product of Israel. | Teva Pharmaceuticals USA, Inc | Class II | Ongoing | 20250212 |
Frequently asked questions
What is Guard used for?
Uses For personal hand hygine to help prevent the spread of bacteria, and can be used in place of hand washing if soap and water are not available.
Who makes Guard?
Apollo Health and Beauty Care is the labeler of record for Guard. 582 FDA label records share the active ingredient ALCOHOL, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.
What form does Guard come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Guard prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Are there other products containing ALCOHOL?
Yes. 582 FDA drug label records list ALCOHOL as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.
Has Guard been recalled?
5 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.