dolce glow body balm
Generic: zinc oxide
Labeler: dolce glow, inc.Drug Facts
Product Profile
Brand Name
dolce glow body balm
Generic Name
zinc oxide
Labeler
dolce glow, inc.
Dosage Form
LOTION
Routes
Active Ingredients
zinc oxide 220 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
83869-2167
Product ID
83869-2167_43cea318-5638-cac7-e063-6394a90af126
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M020
Listing Expiration
2026-12-31
Marketing Start
2025-02-15
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
838692167
Hyphenated Format
83869-2167
Supplemental Identifiers
UNII
Packaging Origin
Original Packager
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
dolce glow body balm (source: ndc)
Generic Name
zinc oxide (source: ndc)
Application Number
M020 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 220 mg/mL
Packaging
- 1 JAR in 1 CARTON (83869-2167-2) / 25 mL in 1 JAR (83869-2167-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "43cea318-5638-cac7-e063-6394a90af126", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["43cea601-a6c0-4de3-e063-6294a90aa8eb"], "manufacturer_name": ["Dolce Glow, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 JAR in 1 CARTON (83869-2167-2) / 25 mL in 1 JAR (83869-2167-1)", "package_ndc": "83869-2167-2", "marketing_start_date": "20250215"}], "brand_name": "Dolce Glow Body Balm", "product_id": "83869-2167_43cea318-5638-cac7-e063-6394a90af126", "dosage_form": "LOTION", "product_ndc": "83869-2167", "generic_name": "Zinc Oxide", "labeler_name": "Dolce Glow, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dolce Glow Body Balm", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "220 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250215", "listing_expiration_date": "20261231"}