Dicopanol
- Manufacturer
- California Pharmaceuticals LLC
- Effective date
- 2016-01-07
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 20:21:48
Label at a glance#
ProductDicopanol
Active ingredientDIPHENHYDRAMINE HYDROCHLORIDE
Label structure5 sections
Label contents#
Full prescribing information#
Instructions for Preparation - page 1
Diphenhydramine - label
Dicopanol. Package Label
Dicopanol - Flavor Suspension label
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| DIPHENHYDRAMINE Pharmacologic Class Indexing | 3 | Indexing - Pharmacologic Class | 20180813 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 0e2e0f88-b076-afe1-4bdd-32bca4375bec | Product name | 3 | 20250127 |
| c6f86816-7da6-43ea-8c25-ac9758311cc5 | Product name | 1 | 20220118 |
| 252e11b6-1a9a-4283-a242-df2c129c496d | Product name | 3 | 20170717 |
| d5e51f11-ad28-caa4-4b49-4143974782ad | Product name | 1 | 20150831 |
| 3e48c9c4-918d-5d23-2f0b-d2398b06be54 | Product name | 1 | 20140508 |
| 865c72dd-0d94-daac-f728-ddd4ded2a79e | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 70332-103-01 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-27a9-f424-e053-dadaa90a57ce | Dicopanol |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70332-103-01 | Dicopanol | 1 in 1 KIT | KIT | 1 | 2 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70332-103-01 | ML - Milliliter | 70332-103 | d153a13f-562a-4c0c-8585-688db5654901 | 1 | 2016-09-02 |
Products#
Every source-derived product name is available through these pages.
- Dicopanol
- Diphenhydramine Hydrochloride
- DIPHENHYDRAMINE
- Oral Suspension Vehicle
- Suspension
- SODIUM CITRATE
- WATER
- GLYCERIN
- XYLITOL
- GLYCYRRHIZIN, AMMONIATED
- PINEAPPLE
- XANTHAN GUM
- SODIUM BENZOATE
- ORANGE
- CITRIC ACID MONOHYDRATE
- MELATONIN
- POTASSIUM SORBATE
- STEVIA LEAF
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 70332-103 | 70332-103-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| DIPHENHYDRAMINE HYDROCHLORIDE | TC2D6JAD40 | ACTIB |
| SODIUM CITRATE | 1Q73Q2JULR | IACT |
| WATER | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| XYLITOL | VCQ006KQ1E | IACT |
| GLYCYRRHIZIN, AMMONIATED | 3VRD35U26C | IACT |
| PINEAPPLE | 2A88ZO081O | IACT |
| XANTHAN GUM | TTV12P4NEE | IACT |
| SODIUM BENZOATE | OJ245FE5EU | IACT |
| ORANGE | 5EVU04N5QU | IACT |
| CITRIC ACID MONOHYDRATE | 2968PHW8QP | IACT |
| MELATONIN | JL5DK93RCL | IACT |
| POTASSIUM SORBATE | 1VPU26JZZ4 | IACT |
| STEVIA LEAF | 6TC6NN0876 | IACT |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 28c7a185-4081-1448-e054-00144ff8d46c | 271bfbb6-4996-500a-e054-00144ff8d46c | 2016-01-07 | 28c7a185-4081-1448-e054-00144ff8d46c 271bfbb6-4996-500a-e054-00144ff8d46c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.




