UltraMax Roll On
- Product NDC
- 10237-900
- 11-digit product format
- 102370900
- Labeler code
- 10237
- Product ID
- 10237-900_3c8fd1f1-f2f1-40ca-9403-3f231a40ca97
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aluminum Zirconium Tetrachlorohydrex Gly
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Church & Dwight Co., Inc.
- Application
- part350
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2000-07-28
- Marketing end
- 0000-00-00
- Substance
- ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
- Active strength
- 21 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record