BINDA BOTANICALS BABY AND KIDS SUNSCREEN SPF50- zinc oxide sunscreen cream

Binda Botanicals Baby and Kids Sunscreen SPF50 by

Drug Labeling and Warnings

Binda Botanicals Baby and Kids Sunscreen SPF50 by is a Otc medication manufactured, distributed, or labeled by VEGANIC SKN LIMITED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Zinc oxide - 25%

PURPOSE

Sunscreen

INDICATIONS & USAGE

kindly refer to label picture

WARNINGS

For external use only.

Do not use on damaged r broken skin.

When using this product keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if rash occurs.

Keep out of reach of children.

If product is swallowed, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

DOSAGE & ADMINISTRATION

Kindly refer to Label

INACTIVE INGREDIENT

See ingredients on label

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BINDA BOTANICALS BABY AND KIDS SUNSCREEN SPF50 
zinc oxide sunscreen cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83252-142
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	25 kg  in 100 kg

Inactive Ingredients
Ingredient Name	Strength
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
XANTHAN GUM (UNII: TTV12P4NEE)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
COCONUT ALKANES (UNII: 1E5KJY107T)
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL (UNII: 3W1JG795YI)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
ISOSTEARIC ACID (UNII: X33R8U0062)
CANDELILLA WAX (UNII: WL0328HX19)
GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83252-142-25	0.1 kg in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	12/05/2025
2	NDC: 83252-142-21	1 kg in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	12/05/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	12/05/2025

Labeler - VEGANIC SKN LIMITED (743536682)

Establishment
Name	Address	ID/FEI	Business Operations
VEGANIC SKN LIMITED		743536682	manufacture(83252-142) , label(83252-142) , pack(83252-142)