OTC - ACTIVE INGREDIENT SECTION
Active Ingredient Purpose
Aluminum Zirconium Tetrachlorohydrex GLY (14.8%).....anti-perspirant
Aluminum Zirconium Tetrachlorohydrex GLY (14.8%).....anti-perspirant
Degree Women UltraClear Pure Rain
- Manufacturer
- Conopco Inc. d/b/a Unilever | Unilever Raeford HPCNA
- Effective date
- 2010-02-02
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 22:23:31
Label at a glance#
ProductDegree Women UltraClear Pure Rain Antiperspirant and Deodorant
Active ingredientAluminum Zirconium Tetrachlorohydrex GLY
Label structure12 sections
Label contents#
Full prescribing information#
WARNINGS SECTION
Warnings
For external use only
For external use only
OTC - DO NOT USE SECTION
Do not use on broken skin
OTC - ASK DOCTOR SECTION
Ask a doctor before use if you have kidney disease
OTC - STOP USE SECTION
Stop use if rash or irritation occurs
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
INACTIVE INGREDIENT SECTION
Cyclopentasiloxane, Stearyl Alcohol, C12-15 Alkyl Benzoate, PPG-14 Butyl Ether, Hydrogenated Castor Oil, Dimethicone, Polyethylene, Fragrance (Parfum), Steareth-100, Helianthus Annuus (Sunflower) Seed Oil, BHT.
OTC - QUESTIONS SECTION
Questions? call 1-866 DEGREE1
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
PDP 2.6 oz
Degree Women Pure Rain 2.6 oz PDP
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
PDP 1.6 oz front
Degree Women Pure Rain 1.6 oz PDP front
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
PDP 1.6 oz back
Degree Women Pure Rain 1.6 oz PDP back
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
0.5oz PDP
Degree Women Pure Rain 0.5 oz PDP
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 64942-0782-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-a90f-f424-e053-dadaa90a57ce | Degree Women UltraClear Pure Rain AP and Deodorant PDP and drug facts |
| 64942-0782-2 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-a90f-f424-e053-dadaa90a57ce | Degree Women UltraClear Pure Rain AP and Deodorant PDP and drug facts |
| 64942-0782-3 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-a90f-f424-e053-dadaa90a57ce | Degree Women UltraClear Pure Rain AP and Deodorant PDP and drug facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 64942-0782-1 | Degree Women UltraClear Pure RainAntiperspirant and Deodorant | 74 g in 1 CONTAINER | STICK | 74 | 1 | |
| 64942-0782-2 | Degree Women UltraClear Pure RainAntiperspirant and Deodorant | 45 g in 1 CONTAINER | STICK | 45 | 1 | |
| 64942-0782-3 | Degree Women UltraClear Pure RainAntiperspirant and Deodorant | 14 g in 1 CONTAINER | STICK | 14 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 64942-0782 | DEGREE WOMEN ULTRACLEAR PURE RAIN ANTIPERSPIRANT AND DEODORANT (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY) STICK [CONOPCO INC. D/B/A UNILEVER] | 1 | Legacy NDC, 3 package rows | 20100203_9bce70e0-a8a5-4867-94ed-64d0d2229f03.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Aluminum Zirconium Tetrachlorohydrex GLY | ACTIVE INGREDIENT | 8O386558JE | 1 | |
| Aluminum Cation | ACTIVE MOIETY | 3XHB1D032B | 1 |
Products#
Every source-derived product name is available through these pages.
- Degree Women UltraClear Pure Rain Antiperspirant and Deodorant
- Aluminum Zirconium Tetrachlorohydrex GLY
- Aluminum Cation
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 64942-0782 | 64942-0782-1, 64942-0782-2, 64942-0782-3 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Aluminum Zirconium Tetrachlorohydrex GLY | 8O386558JE | ACTIB |
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 |
|---|---|---|---|---|---|---|
| 70b6158d-d36a-427a-92fe-f78f6eeebbf1 | 9bce70e0-a8a5-4867-94ed-64d0d2229f03 | 2010-02-02 | Warnings | 70b6158d-d36a-427a-92fe-f78f6eeebbf1 9bce70e0-a8a5-4867-94ed-64d0d2229f03 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.