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NDC 81555-0202-01 CELLANDIR SCALP AMPOULE .05; .3; .25 mg/100mL; mg/100mL; mg/100mL Details
CELLANDIR SCALP AMPOULE .05; .3; .25 mg/100mL; mg/100mL; mg/100mL
CELLANDIR SCALP AMPOULE is a TOPICAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by H.L.C GROUP Co., ltd. The primary component is ALLANTOIN; MENTHOL, UNSPECIFIED FORM; SALICYLIC ACID.
Product Information
| NDC | 81555-0202 |
|---|---|
| Product ID | 81555-202_0ae285fc-b1e6-74b7-e063-6394a90a3cc8 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | CELLANDIR SCALP AMPOULE |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Menthol, Salicylic Acid, Allantoin |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | LIQUID |
| Route | TOPICAL |
| Active Ingredient Strength | .05; .3; .25 |
| Active Ingredient Units | mg/100mL; mg/100mL; mg/100mL |
| Substance Name | ALLANTOIN; MENTHOL, UNSPECIFIED FORM; SALICYLIC ACID |
| Labeler Name | H.L.C GROUP Co., ltd |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH DRUG |
| Application Number | M016 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 81555-0202-01 (81555020201)
| NDC Package Code | 81555-202-01 |
|---|---|
| Billing NDC | 81555020201 |
| Package | 50 mL in 1 AMPULE (81555-202-01) |
| Marketing Start Date | 2021-05-06 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |