mentholatum natural ice - original, spf 15 original

Generic: dimethicone, octinoxate, octisalate

Labeler: the mentholatum company
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mentholatum natural ice - original, spf 15 original
Generic Name dimethicone, octinoxate, octisalate
Labeler the mentholatum company
Dosage Form STICK
Routes
TOPICAL
Active Ingredients

dimethicone 10 mg/g, octinoxate 75 mg/g, octisalate 50 mg/g

Manufacturer
The Mentholatum Company

Identifiers & Regulatory

Product NDC 10742-3070
Product ID 10742-3070_37f19599-dae1-bdf4-e063-6294a90ae10b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2024-09-01

Pharmacologic Class

Physiologic Effect
skin barrier activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 107423070
Hyphenated Format 10742-3070

Supplemental Identifiers

UNII
92RU3N3Y1O 4Y5P7MUD51 4X49Y0596W
NUI
N0000010282

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name mentholatum natural ice - original, spf 15 original (source: ndc)
Generic Name dimethicone, octinoxate, octisalate (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/g
  • 75 mg/g
  • 50 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 BLISTER PACK (10742-3070-1) / 4.2 g in 1 TUBE
source: ndc

Packages (1)

10742-3070-1 1 TUBE in 1 BLISTER PACK (10742-3070-1) / 4.2 g in 1 TUBE

Ingredients (3)

dimethicone (10 mg/g) octinoxate (75 mg/g) octisalate (50 mg/g)

Linked Drug Pages (1)

Mentholatum Natural Ice - Original, SPF 15 Original ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "37f19599-dae1-bdf4-e063-6294a90ae10b", "openfda": {"nui": ["N0000010282"], "unii": ["92RU3N3Y1O", "4Y5P7MUD51", "4X49Y0596W"], "spl_set_id": ["37dc44aa-17b2-8721-e063-6294a90a34f6"], "pharm_class_pe": ["Skin Barrier Activity [PE]"], "manufacturer_name": ["The Mentholatum Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BLISTER PACK (10742-3070-1)  / 4.2 g in 1 TUBE", "package_ndc": "10742-3070-1", "marketing_start_date": "20240901"}], "brand_name": "Mentholatum Natural Ice - Original, SPF 15 Original", "product_id": "10742-3070_37f19599-dae1-bdf4-e063-6294a90ae10b", "dosage_form": "STICK", "pharm_class": ["Skin Barrier Activity [PE]"], "product_ndc": "10742-3070", "generic_name": "dimethicone, octinoxate, octisalate", "labeler_name": "The Mentholatum Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mentholatum Natural Ice - Original, SPF 15", "brand_name_suffix": "Original", "active_ingredients": [{"name": "DIMETHICONE", "strength": "10 mg/g"}, {"name": "OCTINOXATE", "strength": "75 mg/g"}, {"name": "OCTISALATE", "strength": "50 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240901", "listing_expiration_date": "20261231"}