HI AND DRI ANTIPERSPIRANT
- Product NDC
- 10967-057
- 11-digit product format
- 109670057
- Labeler code
- 10967
- Product ID
- 10967-057_3222fd3d-5e0c-40ac-ad46-9bef480bafab
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALUMINUM CHLOROHYDRATE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Revlon Consumer Products Corp
- Application
- part350
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 1982-01-01
- Marketing end
- 0000-00-00
- Substance
- ALUMINUM CHLOROHYDRATE
- Active strength
- 0 g/mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10967-057-97 | HI AND DRI ANTIPERSPIRANTROLL-ON POWDER FRESH | 50 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 50 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10967-057 | HI AND DRI ANTIPERSPIRANT ROLL-ON POWDER FRESH (ALUMINUM CHLOROHYDRATE) LIQUID [REVLON CONSUMER PRODUCTS CORP] | 1 | Legacy NDC, 1 package rows | 20131209_8a7149f6-2e72-4f49-a265-34747172588e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 10967-057-97 | 10967005797 | 50 mL in 1 BOTTLE, WITH APPLICATOR | 50 ml | Historical |