OLP ANTI-ITCH ALLERGY RELIEF
- Product NDC
- 70648-133
- 11-digit product format
- 706480133
- Labeler code
- 70648
- Product ID
- 70648-133_7b9c7090-9720-809c-e053-2a91aa0ab42d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- diphenhydramine
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- OHIO LAB PHARMA LLC.
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-02-21
- Marketing end
- 0000-00-00
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE
- Active strength
- 10 mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 70648-133-01 | OLP ANTI-ITCH ALLERGY RELIEF | 20 g in 1 TUBE | CREAM | 20 | | 2 |
| 70648-133-01 | OLP ANTI-ITCH ALLERGY RELIEF | 1 in 1 CARTON | CREAM | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70648-133 | OLP ANTI-ITCH ALLERGY RELIEF (DIPHENHYDRAMINE) CREAM [OHIO LAB PHARMA LLC.] | 2 | Legacy NDC, 2 package rows | 20181127_65d4acc8-6936-3fd3-e053-2991aa0ab3d3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 70648-133-01 | 70648013301 | 20 g in 1 TUBE | 20 g | Historical |