Right Guard X Antiperspirant and Deodorant DrySpray Fresh Blast
- Manufacturer
- Thriving Brands LLC
- Effective date
- 2026-01-28
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-06-01 01:35:18
Label at a glance#
ProductRight Guard X Antiperspirant and Deodorant DrySpray Fresh Blast
Active ingredientALUMINUM CHLOROHYDRATE
Label structure10 sections
Label contents#
Full prescribing information#
WARNINGS SECTION
INACTIVE INGREDIENT SECTION
INDICATIONS & USAGE SECTION
OTC - ACTIVE INGREDIENT SECTION
OTC - ASK DOCTOR SECTION
OTC - DO NOT USE SECTION
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
OTC - PURPOSE SECTION
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 82699-006-01 | Right Guard X Antiperspirant and Deodorant DrySpray Fresh Blast | 107 g in 1 CANISTER | AEROSOL, SPRAY | 107 | 3 |
Products#
Every source-derived product name is available through these pages.
- Right Guard X Antiperspirant and Deodorant DrySpray Fresh Blast
- ALUMINUM CHLOROHYDRATE
- CYCLOMETHICONE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 82699-006 | 82699-006-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALUMINUM CHLOROHYDRATE | HPN8MZW13M | ACTIB |
| CYCLOMETHICONE | NMQ347994Z | 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 |
|---|---|---|---|---|---|---|
| Right Guard X Antiperspirant and Deodorant DrySpray Fresh Blast | RIGHT GUARD X ANTIPERSPIRANT AND DEODORANT DRYSPRAY FRESH BLAST | Thriving Brands LLC | 05aa1a1a-9e51-2781-e063-6394a90aef6b | 2026-01-28 | Warnings | 82699-006-01 82699-006 82699000601 4978fb3c-5b0e-f893-e063-6294a90aa147 05aa1a1a-9e51-2781-e063-6394a90aef6b |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
