OXYMETAZOLINE HYDROCHLORIDE
- Product NDC
- 63868-676
- 11-digit product format
- 638680676
- Labeler code
- 63868
- Product ID
- 63868-676_3446fcd3-f2b4-4f5f-b80e-f0600b7efc81
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OXYMETAZOLINE HYDROCHLORIDE
- Dosage form
- SPRAY
- Route
- NASAL
- Labeler
- CHAIN DRUG MARKETING ASSOCIATION INC.
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-02-01
- Substance
- OXYMETAZOLINE HYDROCHLORIDE
- Active strength
- .05 g/100mL
- Pharmacologic classes
- Imidazolines [CS], Increased Sympathetic Activity [PE], Vasoconstriction [PE], Vasoconstrictor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- OXYMETAZOLINE HYDROCHLORIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OXYMETAZOLINE HYDROCHLORIDE | .05 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | K89MJ0S5VY |
| Rxcui | 1000990 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63868-676-01 | OXYMETAZOLINE HYDROCHLORIDE | 30 mL in 1 BOTTLE, SPRAY | SPRAY | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63868-676 | OXYMETAZOLINE HYDROCHLORIDE SPRAY [CHAIN DRUG MARKETING ASSOCIATION INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20241228_c7b1f980-9b0d-4f63-a70d-fd366658f863.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63868-676-01 | 63868067601 | 30 mL in 1 BOTTLE, SPRAY (63868-676-01) | 30 ml | 2021-02-01 | 0000-00-00 | No | No | Current |