Itch Relief
- Product NDC
- 0869-0295
- 11-digit product format
- 008690295
- Labeler code
- 0869
- Product ID
- 0869-0295_f80ff737-021f-41bd-bfec-3ae3f9eafd85
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine HCl, Zinc Acetate
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Vi-Jon, LLC
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2010-07-14
- Marketing end
- 0000-00-00
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE
- Active strength
- 18 mg/mL; mg/mL
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0869-0295-20 | 00869029520 | 59 mL in 1 BOTTLE, SPRAY (0869-0295-20) | 59 ml | 2010-07-14 | 0000-00-00 | No | No | Current |