Over-the-counter drug · OTC MONOGRAPH DRUG
QIDILA Whitening Skin Lightening Cream NDC 85212-0006
Tocopherol 1 g/100mL + 5 more ingredients · Cream · Extracorporeal · Beijing JUNGE Technology Co., Ltd.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 85212-0006-1 | 8521200060185212000601 | 30 mL in 1 BOTTLE (85212-0006-1)Marketed from Jan 1, 2025 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- QIDILA Whitening Skin Lightening Cream
- Generic name (nonproprietary)
- butylene glycol,butyrospermum parkii (shea butter),kyounin yu,tocopherol,ascorbic acid,niacinamide
- Active ingredients
- Tocopherol — 1 g/100mLButyrospermum parkii (Shea) butter — 3 g/100mLPrunus armeniaca (Apricot) kernel extract — 2 g/100mLNiacinamide — .05 g/100mLButylene glycol — 5 g/100mLAscorbic acid — .05 g/100mL
- Dosage form
- Cream
- Route
- Extracorporeal
- Labeler
- Beijing JUNGE Technology Co., Ltd.NDC labeler code 85212
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Other FDA classes
- Ascorbic Acid (Chemical structure)
- Identifiers
- Product ID 85212-0006_2e66a508-3f57-4500-e063-6394a90aaa9dSPL ID 2e66a508-3f57-4500-e063-6394a90aaa9dSPL set ID 2e66a508-3f56-4500-e063-6394a90aaa9dUNII R0ZB2556P8, K49155WL9Y, 75356789IW, 25X51I8RD4, 3XUS85K0RA, PQ6CK8PD0R
- Pharmacologic class
- Vitamin C
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.
- NDC on a medical claim
N485212000601followed by a unit qualifier and the quantityPackage 85212-0006-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Uses 1 .Clean and dry your skin. 2 . Apply a proper amount of the cream on desired area with your fingers, using a circular motion to massage the cream into the skin. 3 .Please apply it twice a day(morning and evening)
Excerpt only. Read the full label for complete information.
About NDC 85212-0006
- What is NDC 85212-0006?
- 85212-0006 is the product NDC for QIDILA Whitening Skin Lightening Cream, Tocopherol 1 g/100mL + 5 more ingredients cream, listed with the FDA by Beijing JUNGE Technology Co., Ltd.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- QIDILA Whitening Skin Lightening Cream (Butylene glycol,Butyrospermum parkii (Shea butter),Kyounin yu,Tocopherol,Ascorbic acid,Niacinamide).
- What is the active ingredient?
- Tocopherol, Butyrospermum parkii (Shea) butter, Prunus armeniaca (Apricot) kernel extract, Niacinamide, Butylene glycol, Ascorbic acid.
- Who is the labeler?
- Beijing JUNGE Technology Co., Ltd., NDC labeler code 85212. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for QIDILA Whitening Skin Lightening Cream?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Other NDCs under 505G(a)(3)
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
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