warnings
Warnings For external use only Do not use on broken skin Ask a doctor before use if you have kidney disease Stop use if rash occurs Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
AVON Far Away Voyage Roll-On Anti-Perspirant Deodorant
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- AVON Far Away Voyage Roll-On Anti-Perspirant Deodorant
- Generic name
- ALUMINUM CHLOROHYDRATE
- Manufacturer
- Avon Cosmetics Manufacturing, S. de R.L. de C.V.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 25259b6c-1394-49c5-e063-6294a90a26a2
- SPL ID
- 258e5854-cf2c-8a0f-e063-6394a90a4d08
- Version
- 2
- Effective date
- 2024-10-28
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:19:36
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M019 | openfda.application_number | |
| brand name | AVON Far Away Voyage Roll-On Anti-Perspirant Deodorant | openfda.brand_name | |
| generic name | ALUMINUM CHLOROHYDRATE | openfda.generic_name | |
| manufacturer name | Avon Cosmetics Manufacturing, S. de R.L. de C.V. | openfda.manufacturer_name | |
| ndc | package | 71110-1512-1 | openfda.package_ndc |
| ndc | product | 71110-1512 | openfda.product_ndc |
| ndc11 | package | 71110151201 | derived:openfda.package_ndc |
| spl id | 258e5854-cf2c-8a0f-e063-6394a90a4d08 | id | |
| spl set id | 25259b6c-1394-49c5-e063-6294a90a26a2 | set_id | |
| unii | HPN8MZW13M | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.