OTC - ACTIVE INGREDIENT SECTION
Active Ingredient ........................................................................... Purpose
Aluminum Chlorohydrate 23.3% .................................................. Antiperspirant
Antiperspirant Dry 1.6 oz Lady
- Manufacturer
- Rejoice International Inc. | Sanit & Sons Company Limited
- Effective date
- 2020-01-13
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:02:54
Label at a glance#
ProductAntiperspirant Dry 1.6 oz Lady Antiperspirant
Active ingredientALUMINUM CHLOROHYDRATE
Label structure8 sections
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
Antiperspirant
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
INDICATIONS & USAGE SECTION
Reduces underarm wetness
WARNINGS SECTION
Warnings
For external use only.
Flammable.
Do not spray near flame or while smoking.
Contents under pressure
Do not crush, puncture or incinerate container.
Do not expose to heat or store at temperatures above 120oF
Do not use on broken skin.
Ask a doctor before using, if you have kidney disease.
When using this product
Keep away from face and mouth to avoid breathing it. Avoid spraying in eyes.
Use only directed. Intentional missuse by deliberately concentrating and inhaling the contents can be harmful or fatal
Stop use if rash or irritation develops.
DOSAGE & ADMINISTRATION SECTION
Directions
- For underarm use only. Shake can well before each use. Hold can 6 inches away from skin. Spray underarm.
INACTIVE INGREDIENT SECTION
Inactive Ingredients
Isobutane, Butane, Hydrofluorocarbon 152a, Cyclopentasiloxane, Ethyl Alcohol, PPG-14 Butyl Ether, Helianthus Annuus Seed Oil, Isopropryl Myristate, C12-15 Alkyl Benzoate, Frangrance, Propane, Aluminum Starch Ocetenylsuccinate, Disteardimonium Hectorite, Dimethicone, Tocopheryl Acetate, BHT, Silica
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 57337-106-01 | 2021-07-23 | C162847 | 48780-1 | c7ccaba7-24ba-fd44-e053-dadaa90aa01b | Antiperspirant Dry 1.6 oz Lady |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 57337-106-01 | Antiperspirant Dry 1.6 oz LadyAntiperspirant | 45 g in 1 BOTTLE, SPRAY | AEROSOL, SPRAY | 45 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Antiperspirant Dry 1.6 oz Lady Antiperspirant
- Aluminum Chlorohydrate
- ISOPROPYL MYRISTATE
- ALUMINUM STARCH OCTENYLSUCCINATE
- DISTEARDIMONIUM HECTORITE
- CYCLOMETHICONE 5
- PPG-14 BUTYL ETHER
- ALKYL (C12-15) BENZOATE
- ALCOHOL
- BUTYLATED HYDROXYTOLUENE
- ISOBUTANE
- 1,1-DIFLUOROETHANE
- SUNFLOWER OIL
- PROPANE
- LAURYL PHOSPHATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 57337-106 | 57337-106-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| 9c0d8c82-6c4d-a511-e053-2995a90a793f | 9c0d5f62-a757-7ab7-e053-2995a90a47d9 | 2020-01-13 | Warnings | 9c0d8c82-6c4d-a511-e053-2995a90a793f 9c0d5f62-a757-7ab7-e053-2995a90a47d9 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.