Drugplain

AnubisMed .15 g/50mL

Sodium Bicarbonate, Aloe Barbadensis Leaf Juice, Imidazolidinyl Urea · LIQUID · ANUBIS COSMETICS SL

No Recall HistoryCurrently in Shortage
Plain English

Anubismed is a topical liquid product containing sodium bicarbonate and aloe that is available over-the-counter for skin care use. This product is classified as a standardized chemical allergen preparation.

Key Facts

Brand Name
AnubisMed
Generic Name
Sodium Bicarbonate, Aloe Barbadensis Leaf Juice, Imidazolidinyl Urea
NDC Code (Product)
83021-400
Manufacturer
ANUBIS COSMETICS SL
Strength
.15 g/50mL
Dosage Form
LIQUID
Route
TOPICAL
Marketing Status
Application #
M016
Drug Class
Standardized Chemical Allergen [EPC]
Marketing Start
10/26/2022

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

AnubisMed 50+ Protection Fluid Indications and Usage

Dosage & Administration

how to use

Warnings

warnings

Frequently Asked Questions

What is AnubisMed used for?

Anubismed is a topical liquid product containing sodium bicarbonate and aloe that is available over-the-counter for skin care use. This product is classified as a standardized chemical allergen preparation.

Is AnubisMed a controlled substance?

AnubisMed is not classified as a controlled substance by the DEA.

What is the generic name for AnubisMed?

The generic name for AnubisMed is Sodium Bicarbonate, Aloe Barbadensis Leaf Juice, Imidazolidinyl Urea. There are no other listed brand versions of Sodium Bicarbonate, Aloe Barbadensis Leaf Juice, Imidazolidinyl Urea.

What is the NDC code for AnubisMed .15 g/50mL?

The NDC (National Drug Code) for AnubisMed .15 g/50mL is 83021-400, listed by ANUBIS COSMETICS SL.

Product NDC

83021-400

Package NDC

83021-400-50

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)