Shelo Nabel Baba De Caracol
Product Images NDC 71424-1222

8 FDA label images from Corporativo Serysi S De R L De C V · 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 Baba De Caracol (NDC 71424-1222). 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

Display Panel U222

Display Panel U222
Label for Shelo NABEL Baba de Caracol hand lotion by Corporativo Serysi S de R L de C V. The blue label indicates it is a 5.07 fl oz (149.93 ml) skin protectant lotion containing 0.5% allantoin. The label notes the allantoin is sourced from herbal ingredients, not snail slime, and the product is made in Mexico.*
FDA Label Image

Indications U222

Indications U222
Label of Shelo NABEL Baba de Caracol hand lotion, indicating Allantoin 0.5% as an active ingredient. The label is bilingual in English and Spanish, describing the product as a skin protectant (Protector de Piel) and lotion for hands (Loción para Manos). The label is blue with white text.*
FDA Label Image

Active Ingredient U222 (Otc Active Ingredient)

Active Ingredient U222 (Otc   Active Ingredient)
A drug facts panel listing the active ingredient Allantoin 0.5% as a skin protectant, displayed in English and Spanish. It shows 'Active Ingredient / Ingrediente Activo' and 'Purpose / Propósito' headings with corresponding information underneath.*
FDA Label Image

Administration U222 (Otc Directions Section)

Administration U222 (Otc   Directions Section)
A bilingual directions panel in English and Spanish for Shelo NABEL Baba de Caracol. It instructs users to apply the product generously on hands and massage gently for greater absorption, with the Spanish translation provided.*
FDA Label Image

Inactive Ingredient U222 (Otc Inactive Ingredient U222)

Inactive Ingredient U222 (Otc   Inactive Ingredient U222)
This text panel lists the inactive ingredients in Shelo NABEL Baba de Caracol. Ingredients include distilled water, silicone oil, laureth 3, polysorbate 20, isopropyl palmitate, stearic acid, cetostearyl alcohol, acrylate copolymer sodium, liquid paraffin, PPG 1-Trideceth-6, phenoxyethanol, DMDM hydantoin, benzyl alcohol, and hydroxyacetophenone. The list is presented in both English and Spanish.*
FDA Label Image

Indications U222 (Otc Keep Reach Out Of Children)

Indications U222 (Otc   Keep Reach Out Of Children)
A bilingual safety warning panel with the message 'Keep out of the reach of children / Mantener fuera del alcance de los niños.' The text is presented in both English and Spanish in bold font on a white background with a black border line above and below the text.*
FDA Label Image

Purpose U222 (Otc Purpose Use)

Purpose U222 (Otc   Purpose Use)
A bilingual (English and Spanish) text panel titled 'Uses / Uso' stating that the product temporarily protects and helps relieve chapped or cracked skin.*
FDA Label Image

Warnings U222 (Warnings And Precautions)

Warnings U222 (Warnings And Precautions)
A bilingual warnings label panel in English and Spanish for Shelo NABEL Baba de Caracol. It includes instructions about external use only, keeping out of reach of children, prohibited uses such as on deep wounds or animal bites, precautions when using the product including avoiding eye contact, and advice to stop use and seek medical attention if irritation or worsening symptoms occur. It also advises contacting a Poison Control Center immediately if swallowed.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.