Shelo Nabel Crema Baba De Caracol
Product Images NDC 71424-1001

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Shelo Nabel Crema Baba De Caracol (NDC 71424-1001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Corporativo Serysi S De R L De C V, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Administration U001 (Administration)

Administration U001 (Administration)
This is a set of instructions for applying a product, likely a facial cream or lotion, to a clean face using circular motions from the center of the face outwards. The instructions are given both in English and Spanish.*
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Display Panel

Display Panel
This is a skincare product called BABADE CARAG®L that comes in a facial lotion form and is designed to function as a skin protectant. It contains 1% Allantoin/Alantoina and has a net content of 9.30 floz/275.03 mt. The product packaging indicates it has a facial lotion in it and is a protector de piel (skin protector) too.*
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Inactive Ingredients U001 (Inactive Ingredients)

Inactive Ingredients U001 (Inactive Ingredients)
The text describes the inactive ingredients present in a product. The ingredients include distilled water, glycerin, isopropyl Palmitate, Sorbate 20, Polysorbate 20, Carbomer 940, Triethanolamine, fragrance, Phenoxyethanol, DMDM Hydantoin, Benzyl Alcohol, and Hydroxyacetophenone. The same information is provided in Spanish.*
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Indications U001

Indications U001
Uses: Temporarily protects and helps relieve chapped or cracked skin. Translation: Utiliza: Protege temporalmente y ayuda a aliviar la piel agrietada o reseca. Description: This product provides temporary relief and protection for chapped or cracked skin.*
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Koroc U001 (Koroc)

FDA Label Image

Active Ingredient U001 (Otc Active Ingredient Section)

Active Ingredient U001 (Otc   Active Ingredient Section)
This is a description of an active ingredient called Allantoin, which is present at 1%. It is used as a skin protectant. The purpose of this ingredient is mentioned as protecting the skin.*
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Purpose U001

FDA Label Image

Warnings U001 (Warnings And Precaution Section)

Warnings U001 (Warnings And Precaution Section)
This is a warning label for a product that can only be used externally. It advises to keep the product out of the reach of children and avoid using it on deep wounds, animal bites, or serious burns. Furthermore, it warns not to let the product come in contact with the eyes and to seek medical attention if the product causes irritation or sensitivity, or if symptoms last for more than a week or reoccur within a few days. If swallowed, it advises to seek medical help immediately or contact a Poison Control Center.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.