Allergy Relief
- Product NDC
- 71335-2812
- 11-digit product format
- 713352812
- Labeler code
- 71335
- Product ID
- 71335-2812_72e5155f-440e-47b0-b1f9-3c6efa51f71b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Chlorpheniramine maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-04-22
- Substance
- CHLORPHENIRAMINE MALEATE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| V1Q0O9OJ9Z | CHLORPHENIRAMINE MALEATE | 113-92-8 | CHLORPHENIRAMINE MALEATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2812-1 | 71335281201 | 1 BOTTLE, PLASTIC in 1 CARTON (71335-2812-1) / 100 TABLET in 1 BOTTLE, PLASTIC | 2025-10-15 | No | No | Historical |